Directed β-C(sp.SUP.3.)#H iodination and arylation of ketones
10875822 · 2020-12-29
Assignee
Inventors
Cpc classification
C07C255/64
CHEMISTRY; METALLURGY
B01J2531/0219
PERFORMING OPERATIONS; TRANSPORTING
C07C249/12
CHEMISTRY; METALLURGY
B01J31/2226
PERFORMING OPERATIONS; TRANSPORTING
C07F7/1892
CHEMISTRY; METALLURGY
C07C2602/42
CHEMISTRY; METALLURGY
C07C253/30
CHEMISTRY; METALLURGY
C07C251/60
CHEMISTRY; METALLURGY
C07C249/12
CHEMISTRY; METALLURGY
C07C255/64
CHEMISTRY; METALLURGY
C07C253/30
CHEMISTRY; METALLURGY
International classification
Abstract
This invention discloses the first example of palladium(II)-catalyzed -C(sp.sup.3)-H iodination or arylation of a wide range of ketones by using a commercially available aminooxyacetic acid auxiliary. This L, X-type directing group overcomes the limitation of the transient directing group approach for -C(sp.sup.3)-H functionalization of ketones. Practical advantages of this method include simple installation of the auxiliary without chromatography, exceptional tolerance of a-functional groups, double bonds and triple bonds and rapid access to diverse sterically hindered quaternary centers.
Claims
1. A method of -C(sp.sup.3)-H iodination of a ketone having a p-hydrogen substituent, comprising: contacting the ketone and an aminooxyacetic acid in pyridine solvent to provide the corresponding oxime; then, contacting the oxime with iodine in the presence of a palladium(II) salt and phenyliodoniumacetate, in an aprotic solvent; then, hydrolyzing the oxime group under acidic conditions to provide the product -C(sp.sup.3)-iodoketone.
2. The method of claim 1 wherein the aminooxyacetic acid is aminooxyacetic acid or 2,2-dimethylaminooxyacetic acid.
3. The method of claim 1 wherein the palladium(II) salt is palladium(II) acetate or palladium(II)trifluoroacetate.
4. The method of claim 1 wherein the aprotic solvent is dioxane or 1,1,1,3,3,3-hexafluoroisopropanol.
5. The method of claim 1 wherein the oxime group is hydrolyzed in a solution of concentrated hydrochloric acid in dioxane.
6. A method of -C(sp.sup.3)-H arylation of a ketone having a -hydrogen substituent, comprising: contacting the ketone and an aminooxyacetic acid in pyridine solvent to provide the corresponding oxime; then, contacting the oxime with an aryl iodide and silver trifluoroacetate in the presence of a palladium(II) salt, in an aprotic solvent; then, hydrolyzing the oxime group under acidic conditions to provide the product -C(sp.sup.3)-arylketone.
7. The method of claim 6 wherein the aminooxyacetic acid is aminooxyacetic acid or 2,2-dimethylaminooxyacetic acid.
8. The method of claim 6 wherein the palladium(II) salt is palladium(II) acetate or palladium(II)trifluoroacetate.
9. The method of claim 6 wherein the aprotic solvent is dioxane or 1,1,1,3,3,3-hexafluoroisopropanol.
10. The method of claim 6 wherein the oxime group is hydrolyzed in a solution of concentrated hydrochloric acid in dioxane.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) FIG. 1. Scheme 1 shows transient and covalent directing groups based on amino acids
(2) FIG. 2. Table 1. Directing group evaluation for C(sp.sup.3)-H iodination.
(3) FIG. 3. Scheme 4 showing characterization of the palladacycle.
DETAILED DESCRIPTION
(4) Herein, we report a practical directing group that enables the -iodination and the -arylation of ketones. The combination of the imino-carboxylic acid chelation established in our previous transient directing group in concert with the stability of an oxime linkage successfully overcomes the limitations of previous directing groups, presumably generating a highly active Pd precursor. Consequently, The substrate scope herein reported is significantly broader than previously reported C(sp.sup.3)-H functionalizations of ketones.
(5) The use of amino acid transient directing groups for the -C(sp.sup.3)-H functionalization of ketones is appealing from the viewpoint of step-economy. However, the free amino acid used is often incompatible with a range of oxidants or coupling reagents preventing the development of a diverse range of transformations. Since the bidentate imino-carboxyl chelation has been shown to be effective in directing C(sp.sup.3)-H activation,.sup.6 we proposed to replace the imine by a more stable oxime.sup.8 motif to render the linkage irreversible (FIG. 1; Scheme 1).
(6) Importantly, L, X-type (i.e. neutral, anionic) directing groups have a fundamental advantage over the L, L (i.e. neutral, neutral) counterparts as shown in Scheme 2. Using L, L-type directing groups, a CH bond must displace an acetate to form a thermodynamically unfavorable cationic Pd(II) species in order to achieve C-H insertion. (Scheme 2. Eq 2).
(7) Furthermore, the weakly coordinating nature of the carboxylic acid is also beneficial for the reactivity of the C-H insertion intermediate compared to other highly stable bidentate complexes.
(8) ##STR00001##
(9) To test this design principle, we chose -C(sp.sup.3)-H iodination as the model reaction for two reasons: First, C(sp.sup.3)-H iodination of ketones remains an unsolved problem except for a single example of stoichiometric iodination reaction of oxime reported by Sutherland in 1984..sup.2b Second, -iodoketones are extremely versatile synthons, yet the synthesis of -iodoketones is a well-known challenge, especially for sterically hindered -quaternary ketones..sup.9 Therefore, the model substrate 1a-1 was readily prepared by the condensation between pinacolone and commercially available aminooxyacetic acid under mild conditions in high yield without chromatography. Guided by our previous study of oxazoline- and acidic amide-directed -C(sp.sup.3)-H iodination of carboxylic acid substrates,.sup.5,10 we found that treating model substrate 1a-1 with 1 equiv I.sub.2, Phl(OAc).sub.2 and 10 mol % Pd(OAc).sub.2 in 1,4-dioxane gave the desired iodination product in 70% yield. The use of other solvents gave significantly lower yields. Replacing Pd(OAc).sub.2 with Pd(TFA).sub.2 improved the yield to 88% (FIG. 2; Table 1).
(10) Importantly, reducing catalyst loading to 5 mol % did not result in a noticeable decrease in yield. The observed high reactivity prompted us to investigate the coordination mode of the directing group and the impact of the structures on the reactivity. The corresponding L, L-type directing group bearing the methyl ester (DG2) gave poor yield which confirms the superiority of the L, X-type auxiliary (Scheme 2. Eq 1-2). Enhancing the bidentate coordination (due to the Thorp-Ingold effect) led to drastic increase in di- and tri-iodination products (2a-3), which is likely due to slow dissociation from Pd. Considering the well-established efficiency of the acidic amide directing group,.sup.11 we also converted the carboxylic acid into amides (DG4 and DG5). Although DG4 has comparable reactivity, the stronger binding affinity led to predominant formation of the tri-iodinated products. As expected, the less acidic amide DG5 is not as reactive, presumably due to its inability to adopt L, X-type coordination.
(11) With the optimal directing group and reaction conditions established, we evaluated the scope of C(sp.sup.3)-H iodination. It is worth highlighting the practical advantage of this directing group: preparation of a wide range of substrates was performed using the commercially available aminooxyacetic acid without chromatography. As shown in Table 2, a variety of alkyl substituted ketones were -iodinated in good-to-excellent yields (2a-d). Note that the quaternary centers in products 2a-c and 2e-h are inaccessible via classic enolate alkylation methods as alkylation of the -methyl group is kinetically favored;.sup.1 all of these products were formed in good-to-excellent yields. The bicyclic natural product Fenchone was iodinated with excellent mono-selectivity despite the presence of three -methyl groups (2d). Notably, aromatic moieties trans to the carboxyl directing moiety were compatible with iodination conditions and no C(sp.sup.2)-H iodination was detected (2e-g, 2o). Ketone derived from Gemfibrozil was iodinated at -methyl group and aromatic ring (2h). Various aromatic rings cis to the carboxyl directing moiety remains intact during the iodination reaction (2i-k, 2p-r). Remarkably, no -iodination was observed in the presence of acidic -hydrogen,.sup.12 only -C(sp.sup.3)-H iodinated products were obtained (2k-m). Again, the quaternary centers in these products cannot be formed using enolate alkylation, which prefers the even more acidic and less hindered -positions..sup.1 Finally, a variety of functional groups at the -position, including nitriles, esters, TBS-protected hydroxyl, alkenyl, and alkynyl groups, were tolerated (2l-r), exhibiting significantly broader substrate scope than previously reported oxime-directed C(sp.sup.3)-H functionalizations.
(12) TABLE-US-00001 TABLE 2 C(sp.sup.3)H Iodination of Ketones.sup.a,b,c
(13) This new auxiliary offers a number of practical advantages over previously developed imine directing groups..sup.2-5 Most importantly, imino-carboxyl directing group displayed superior reactivity over O-methyl oxime directing group with various substrates containing phenyl group, strained rings, alkenes, and other functional groups (Scheme 3).
(14) ##STR00022##
(15) Previous attempts to isolate the C-H insertion intermediate with our previous transient amino acid directing groups were not successful due to the instability of the imine linkage. With the more stable oxime linkage, we were pleased to observe the formation of the C-H insertion intermediate by stirring the substrate 1a with 1.2 equivalents of Pd(OAc).sub.2 in HFIP at 80 C. We were able to isolate a stable complex by trapping with PPh.sub.3 in 81% yield (FIG. 3; Scheme 4). The structure was confirmed by X-ray crystallography. This intermediate provides the first direct evidence for the L, X-coordination mode of the imino-carboxylic acid directing group, confirming the unique role of the carboxyl group as a directing moiety.
(16) ##STR00023##
(17) The oxime auxiliary can be cleaved following iodination using standard acid hydrolysis techniques to yield the iodinated ketone product in good yield. See the Examples section.
(18) In summary, C(sp.sup.3)-H iodination of ketones was developed using a commercially available aminooxyacetic acid auxiliary. This reaction features facile installation and removal of the auxiliary. The substrate scope is significantly broader than the previously reported C-H functionalizations of ketones using various approaches. The characterization of the C-H insertion intermediate also provides the first direct evidence for the L, X-type coordination mode of the imine-carboxylic acid directing groups.
(19) C(sp.sup.3)-H Arylation of Ketones
(20) ##STR00024##
(21) The new oxime directing group can also be used in the formation of -arylketones by an analogous route. Formation of the oxime is followed by reaction with the Pd(II) salt and coupling with an aryl iodide in the presence of silver trifluoroacetate in hexafluoroisopropanol, and the resulting arylated product is worked up as before with formation of the methyl ester of the oxime carboxylic acid. Cleavage of the oxime to yield the -arylated ketone is carried out as described above.
DOCUMENTS CITED
(22) (1) Cano, R.; Zakarian, A.; McGlacken, G. P. Angew. Chem., Int. Ed. 2017, DOI: 10.100.sup.2/anie.201703079. (2) For selected examples of stoichiometric palladation reactions: (a) Constable, A. G.; McDonald, W. S.; Sawkins, L. C.; Shaw, B. L. J. Chem. Soc. Chem, Commun. 1978, 1061. (b) Carr, K.; Sutherland, J. K. J. Chem. Soc. Chem, Commun. 1984, 1227. (c) Baldwin, J. E.; Najera, C.; Yus, M. J. Chem. Soc. Chem, Commun. 1985, 126. (d) Baldwin, J. E.; Jones, R. H.; Najera, C.; Yus, M. Tetrahedron 1985, 41, 699. (3) For early examples of Pd-catalyzed C(sp.sup.2)-H Halogenation: (a) Fahey, D. R. J. Organomet. Chem. 1971, 27, 283. (b) Andrienko, O. S.; Goncharov, V. S.; Raida, V. S. Russ. J. Org. Chem. 1996, 32, 89. (4) For advances of catalytic C(sp.sup.3)-H activation by using oxime directing group: (a) Desai, L. V.; Hull, K. L.; Sanford, M. S. J. Am. Chem. Soc. 2004, 126, 9542. (b) Thu, H.-Y.; Yu, W.-Y.; Che, C.-M. J. Am. Chem. Soc. 2006, 128, 9048. (c) Kang, T.; Kim, Y.; Lee, D.; Wang, Z.; Chang, S. J. Am. Chem. Soc. 2014, 136, 4141. (d) Gao, P.; Guo, W.; Xue, J.; Zhao, Y.; Yuan, Y.; Xia, Y.; Shi, Z. J. Am. Chem. Soc. 2015, 137, 12231. (5) For asymmetric C(sp.sup.3)-H iodination directed by chiral oxazoline: Giri, R.; Chen, X.; Yu. J.-Q. Angew. Chem., Int. Ed. 2005, 44, 2112. (6) (a) Zhang, F.-L.; Hong, K.; Li, T.-J.; Park, H.; Yu, J.-Q. Science 2016, 351, 252. (b) Yang, K.; Li, Q.; Liu, Y.; Li, G.; Ge, H. J. Am. Chem. Soc. 2016, 138, 12775. (7) For selected reviews on Pd-catalyzed C(sp.sup.3)-H functionalizations: (a) Daugulis, O.; Do, H.-Q.; Shabashov, D. Acc. Chem. Res. 2009, 42, 1074. (b) Lyons, T. W.; Sanford, M. S. Chem. Rev. 2010, 110, 1147. (c) He, J.; Wasa, M.; Chan, K. S. L.; Shao, Q.; Yu, J.-Q. Chem. Rev. 2017, DOI: 10.102.sup.1/.sub.acs.chemrev.6b00622. (8) Kalia, J.; Raines, R. T. Angew. Chem., Int. Ed. 2008, 47, 7523. (9) Roman, B. I.; Kimpe, N. D.; Stevens, C. V. Chem. Rev. 2010, 110, 5914. (10) For acidic amide-directed C(sp.sup.3)-H iodination: Zhu, R.-Y.; Saint-Denis, T. G.; Shao, Y.; He, J.; Sieber, J. D.; Senanayake, C. H.; Yu, J.-Q. J. Am. Chem. Soc. 2017, 139, 5724. (11) For selected examples: (a) Wasa, M.; Engle, K. M.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 3680. (b) Wasa, M.; Chan, K. S. L.; Zhang, X.-G.; He, J.; Miura, M.; Yu, J.-Q. J. Am. Chem. Soc. 2012, 134, 18570. (c) Li, S.; Chen, G.; Feng, C.-G.; Gong, W.; Yu, J.-Q. J. Am. Chem. Soc. 2014, 136, 5267. (d) Zhu, R.-Y.; He, J.; Wang, X.-C.; Yu, J.-Q. J. Am. Chem. Soc. 2014, 136, 13194. (e) Zhu, R.-Y.; Tanaka, K.; Li, G.-C.; He, J.; Fu, H.-Y.; Li, S.-H.; Yu, J.-Q. J. Am. Chem. Soc. 2015, 137, 7067. (f) Wu, Q.-F.; Shen, P.-X.; He, J.; Wang, X.-B.; Zhang, F.; Shao, Q.; Zhu, R.-Y.; Mapelli, C.; Qiao, J. X.; Poss, M. A.; Yu, J.-Q. Science 2017, 355, 499. (12) For selected exmaples of -iodination for ketones: (a) Bekaert, A.; Barberan, O.; Gervais, M.; Brion, J.-D. Tetrahedron Lett. 2000, 41, 2903. (b) Jereb, M.; Stavber, S.; Zupan, M. Synthesis 2003, 853. (c) Wang, Z.; Yin, G.; Qin, J.; Gao, M.; Cao, L.; Wu, A. Synthesis 2008, 3565.
EXAMPLES
(23) General Information
(24) Ketones were obtained from the commercial sources or synthesized following literature procedures, and used to prepare the corresponding substrates. Aminooxyacetic acid hemihydrochioride was obtained from Combi-Blocks. I.sub.2 was obtained from TCl. Phl(OAc).sub.2 was obtained from Sigma-Aldrich. Solvents were obtained from Sigma-Aldrich, Alfa-Aesar and Acros and used directly without further purification. Analytical thin layer chromatography was performed on 0.25 mm silica gel 60-F254. Visualization was carried out with UV light and Vogel's permanganate. .sup.1H NMR was recorded on Bruker AMX-400 instrument (400 MHz) or Bruker DRX-600 instrument (600 MHz). Chemical shifts were quoted in parts per million (ppm) referenced to 0.0 ppm for tetramethylsilane. The following abbreviations (or combinations thereof) were used to explain multiplicities: s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, br=broad. Coupling constants, J, were reported in Hertz unit (Hz). .sup.13C NMR spectra were recorded on Bruker AMX-400 instrument (100 MHz) or Bruker DRX-600 instrument (150 MHz), and were fully decoupled by broad band proton decoupling. .sup.19F NMR spectra were recorded on Bruker AMX-400 instrument (100 MHz), and were fully decoupled by broad band proton decoupling. Chemical shifts were reported in ppm referenced to either the center line of a triplet at 77.0 ppm of chloroform-d or the center line of a multiplet at 29.84 ppm of acetone-d.sup.6. In the .sup.13C NMR analysis, peaks that correspond to those of the polyfluoroarylamide auxiliary appeared as nearly invisible, complex sets of multiplets; they were omitted in the following spectroscopic analysis. High-resolution mass spectra (HRMS) were recorded on an Agilent Mass spectrometer using ESI-TOF (electrospray ionization-time of flight).
(25) Substrate Structures
(26) ##STR00025## ##STR00026## ##STR00027## ##STR00028##
Experimental Section
Substrate Preparation
(27) Ketones for substrates 1a, 1b, 1d, 1i, 1l, 1m and 1p are commercial available. Ketones for substrates 1e, 1f and 1g were synthesized following literature procedures..sup.1 Ketones for substrates 1c and 1h were synthesized by the reaction between corresponding carboxylic acids and MeLi. The procedure can be found in literature..sup.2 Ketone for substrate 1j was synthesized following literature procedures..sup.3 Ketone for substrate 1k was synthesized following literature procedures..sup.2 Ketones for substrates 1n and 1o were synthesized following literature procedures..sup.4 Ketone for substrate 1q was synthesized following literature procedures..sup.5 Ketone for substrate 1r was synthesized following literature procedures..sup.6
(28) ##STR00029##
Ketone (2 mmol, 1 equiv) and aminooxyacetic acid hemihydrochloride (4 mmol, 437 mg, 2 equiv) were weighed into an oven dried 50 mL round bottom flask with a magnetic stir bar under air. 5 mL Pyridine was added and the mixture was stirred at 60 C. for 2 h. Upon completion, most pyridine was evaporated under vacuum. The resulting mixture was diluted with EtOAc (50 mL) and washed successively with water (100 mL) and diluted HCl aqueous solution (100 mL, ca. 0.01 M). The organic phase was dried with anhydrous Na.sub.2SO.sub.4 and the solvent was removed under vacuum. Notably, the pure compounds were obtained in good yields for all cases without chromatography.
(29) ##STR00030##
(E)-2-(((3,3-dimethylbutan-2-ylidene)amino)oxy)acetic acid (1a)
(30) .sup.1H NMR (600 MHz, CDCl.sub.3) 4.59 (s, 2H), 1.90 (s, 3H), 1.12 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.41, 166.90, 69.93, 37.30, 27.44, 10.88. HRMS (ESI-TOF) Calcd for C.sub.8H.sub.14NO.sub.3.sup. [MH].sup.: 172.0979, found: 172.0972.
(31) ##STR00031##
(E)-2-(((3,3-dimethylpentan-2-ylidene)amino)oxy)acetic acid (1b)
(32) .sup.1H NMR (600 MHz, CDCl.sub.3) 4.58 (s, 2H), 1.86 (s, 3H), 1.47 (q, J=7.2 Hz, 2H), 1.08 (s, 6H), 0.76 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.73, 165.83, 70.05, 40.67, 32.74, 24.97, 10.79, 8.81. HRMS (ESI-TOF) Calcd for C.sub.9H.sub.16NO.sub.3.sup. [MH].sup.: 186.1136, found: 186.1132.
(33) ##STR00032##
(E)-2-(((1-(1-methylcyclohexyl)ethylidene)amino)oxy)acetic acid (1c)
(34) .sup.1H NMR (600 MHz, CDCl.sub.3) 4.60 (s, 2H), 1.88 (s, 3H), 1.82-1.79 (m, 2H), 1.51-1.31 (m, 8H), 1.07 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.06, 166.24, 69.81, 40.78, 35.20, 35.15, 26.05, 25.97, 22.35. HRMS (ESI-TOF) Calcd for C.sub.11H.sub.18NO.sub.3.sup. [MH].sup.: 212.1292, found: 212.1287.
(35) ##STR00033##
2-(((E)-((1S,4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ylidene)amino)oxy)acetic acid (1d)
(36) 1d was synthesized following the general procedures except the reaction temperature is 120 C. and the reaction time is 12 h. .sup.1H NMR (600 MHz, CDCl.sub.3) 4.51 (s, 2H), 1.87-1.84 (m, 1H), 1.81-1.78 (m, 1H), 1.75-1.73 (m, 1H), 1.61-1.59 (m, 2H), 1.44-1.38 (m, 2H), 1.30 (s, 3H), 1.28 (s, 3H), 1.21 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 176.60, 173.20, 69.98, 50.55, 48.49, 45.04, 43.31, 34.19, 25.11, 23.26, 22.47, 16.88. HRMS (ESI-TOF) Calcd for C.sub.12H.sub.18NO.sub.3.sup. [MH].sup.: 224.1292, found: 224.1288.
(37) ##STR00034##
(E)-2-(((3,3-dimethyl-4-phenylbutan-2-ylidene)amino)oxy)acetic acid (1e)
(38) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.27-7.19 (m, 3H), 7.06-7.04 (m, 2H), 4.52 (s, 2H), 2.74 (s, 2H), 1.96 (s, 3H), 1.09 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.64, 165.30, 137.90, 130.26, 127.81, 126.25, 70.12, 46.05, 41.36, 25.11, 11.65. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.8NO.sub.3.sup. [MH].sup.: 248.1292, found: 248.1297.
(39) ##STR00035##
(E)-2-(((3-benzyl-3-methylpentan-2-ylidene)amino)oxy)acetic acid (1f)
(40) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.26-7.23 (m, 2H), 7.21-7.19 (m, 1H), 7.05-7.04 (m, 2H), 4.54 (ABq, J=16.8 Hz, 2H), 2.82 (d, J=13.8 Hz, 1H), 2.67 (d, J=13.8 Hz, 1H), 1.94 (s, 3H), 1.71-1.65 (m, 1H), 1.42-1.36 (m, 1H), 0.99 (s, 3H), 0.80 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 173.94, 164.61, 137.76, 130.27, 127.83, 126.26, 70.01, 45.12, 44.97, 31.10, 20.78, 11.70, 8.64. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.20NO.sub.3.sup. [MH].sup.: 262.1449, found: 262.1442.
(41) ##STR00036##
(E)-2-(((3-ethyl-3-methyl-5-phenylpentan-2-ylidene)amino)oxy)acetic acid (1g)
(42) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.25 (m, 2H), 7.18-7.14 (m, 3H), 4.63 (s, 2H), 2.52 (td, J=5.4 Hz, J=13.2 Hz, 1H), 2.38 (td, J=4.8 Hz, J=13.2 Hz, 1H), 1.86 (s, 3H), 1.83-1.78 (m, 1H), 1.66-1.54 (m, 2H), 1.47-1.41 (m, 1H), 1.12 (s, 3H), 0.78 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.43, 164.66, 142.62, 128.36, 128.25, 125.73, 69.89, 44.07, 41.00, 31.70, 30.77, 20.68, 10.89, 8.38. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.22NO.sub.3.sup. [MH].sup.: 276.1605, found: 276.1609.
(43) ##STR00037##
(E)-2-(((6-(2,5-dimethylphenoxy)-3,3-dimethylhexan-2-ylidene)amino)oxy)acetic acid (1h)
(44) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.00 (d, J=7.2 Hz, 1H), 6.66 (d, J=7.6 Hz, 1H), 6.60 (s, 1H), 4.60 (s, 2H), 3.92-3.88 (m, 2H), 2.30 (s, 3H), 2.17 (s, 3H), 1.90 (s, 3H), 1.66-1.63 (m, 4H), 1.14 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 173.98, 166.02, 156.92, 136.48, 130.28, 123.48, 120.67, 111.88, 69.85, 67.78, 40.31, 36.65, 25.48, 24.78, 21.38, 15.78, 10.85. HRMS (ESI-TOF) Calcd for C.sub.18H.sub.26NO.sub.4.sup. [MH].sup.: 320.1867, found: 320.1862.
(45) ##STR00038##
(Z)-2-(((2,2-dimethyl-1-phenylpropylidene)amino)oxy)acetic acid (1i)
(46) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.42-7.39 (m, 2H), 7.37-7.34 (m, 1H), 7.12-7.10 (m, 2H), 4.51 (s, 2H), 1.17 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.65, 168.26, 127.91, 127.90, 127.35, 127.34, 70.23, 37.48, 28.16. HRMS (ESI-TOF) Calcd for C.sub.13H.sub.16NO.sub.3.sup. [MH].sup.: 234.1136, found: 234.1130.
(47) ##STR00039##
(Z)-2-(((1-(4-methoxyphenyl)-2,2-dimethylpropylidene)amino)oxy)acetic acid (1j)
(48) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.06-7.04 (m, 2H), 6.95-6.92 (m, 2H), 4.54 (s, 2H), 3.82 (s, 3H), 1.16 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.14, 168.57, 159.15, 128.59, 125.62, 113.47, 70.04, 55.14, 37.71, 28.17. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.18NO.sub.4.sup. [MH].sup.: 262.1241, found: 262.1247.
(49) ##STR00040##
(E)-2-(((3,3-dimethyl-1-phenylbutan-2-ylidene)amino)oxy)acetic acid (1k)
(50) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.25 (m, 2H), 7.23-7.22 (m, 2H), 7.19-7.17 (m, 1H), 4.63 (s, 2H), 3.81 (s, 2H), 1.11 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.94, 167.09, 136.77, 128.43, 128.25, 126.08, 69.95, 37.81, 31.80, 28.13. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.18NO.sub.3.sup. [MH].sup.: 248.1292, found: 248.1299.
(51) ##STR00041##
(E)-2-(((1-cyano-3,3-dimethylbutan-2-ylidene)amino)oxy)acetic acid (1l)
(52) .sup.1H NMR (600 MHz, CDCl.sub.3) 4.75 (s, 2H), 3.36 (s, 2H), 1.19 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.19, 157.34, 115.14, 70.19, 37.46, 27.14, 13.66. HRMS (ESI-TOF) Calcd for C.sub.9H.sub.3N.sub.2O.sub.3.sup. [MH].sup.: 197.0932, found: 197.0939.
(53) ##STR00042##
(E)-2-(((1-ethoxy-4,4-dimethyl-1-oxopentan-3-ylidene)amino)oxy)acetic acid (1m)
(54) .sup.1H NMR (600 MHz, CDCl.sub.3) 4.64 (s, 2H), 4.21 (q, J=7.2 Hz, 2H), 3.42 (s, 2H), 1.28 (t, J=7.2 Hz, 3H), 1.12 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 172.06, 170.18, 162.19, 70.92, 62.10, 37.31, 31.53, 26.96, 13.97. HRMS (ESI-TOF) Calcd for C.sub.11H.sub.18NO.sub.5.sup. [MH].sup.: 244.1190, found: 244.1185.
(55) ##STR00043##
(E)-2-(((4-ethoxy-3,3-dimethyl-4-oxobutan-2-ylidene)amino)oxy)acetic acid (1n)
(56) .sup.1H NMR (400 MHz, CDCl.sub.3) 4.65 (s, 2H), 4.16 (q, J=7.2 Hz, 2H), 1.89 (s, 3H), 1.37 (s, 6H), 1.24 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.70, 174.20, 161.35, 70.02, 61.17, 48.95, 23.04, 14.02, 12.46. HRMS (ESI-TOF) Calcd for C.sub.10H.sub.16NO.sub.5.sup. [MH].sup.: 230.1034, found: 230.1030.
(57) ##STR00044##
(E)-2-(((3-benzyl-4-ethoxy-3-methyl-4-oxobutan-2-ylidene)amino)oxy)acetic acid (1o)
(58) .sup.1H NMR (400 MHz, CDCl.sub.3) 7.24-7.20 (m, 3H), 7.09-7.07 (m, 2H), 4.63 (s, 2H), 4.16 (q, J=7.2 Hz, 2H), 3.25 (d, J=13.6 Hz, 1H), 3.06 (d, J=13.6 Hz, 1H), 1.91 (s, 3H), 1.26 (s, 3H), 1.24 (t, J=8.8 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.33, 173.60, 160.37, 136.65, 130.35, 128.01, 126.70, 70.08, 61.24, 53.82, 41.05, 20.19, 14.01, 13.30. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.20NO.sub.5.sup. [MH].sup.: 306.1347, found: 306.1340.
(59) ##STR00045##
(E)-6,6,8,8,9,9-hexamethyl-5-phenyl-3,7-dioxa-4-aza-8-siladec-4-en-1-oic acid (1p)
(60) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.43-7.34 (m, 3H), 7.26-7.24 (m, 2H), 4.57 (s, 2H), 1.48 (s, 6H), 0.77 (s, 9H), 0.02 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 174.26, 165.76, 132.70, 128.17, 128.11, 127.65, 75.58, 70.14, 29.18, 25.75, 18.09, 2.16. HRMS (ESI-TOF) Calcd for C.sub.18H.sub.28NO.sub.4Si.sup. [MH].sup.: 350.1793, found: 350.1790.
(61) ##STR00046##
2-(((E)-((E)-4,4-dimethyl-1-phenylpent-1-en-3-ylidene)amino)oxy)acetic acid (1q)
(62) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.49-7.47 (m, 2H), 7.42 (d, J=16.8 Hz, 1H), 7.38-7.35 (m, 2H), 7.33-7.30 (m, 1H), 6.64 (d, J=16.8 Hz, 1H), 4.67 (s, 2H), 1.24 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 173.28, 163.69, 139.88, 136.47, 128.93, 128.74, 127.00, 116.29. 70.31, 37.70, 28.63. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.18NO.sub.3.sup. [MH].sup.: 260.1292, found: 260.1299.
(63) ##STR00047##
(Z)-2-(((4,4-dimethyl-1-phenylpent-1-yn-3-ylidene)amino)oxy)acetic acid (1r)
(64) .sup.1H NMR (600 MHz, CDCl.sub.3) 7.54-7.52 (m, 2H), 7.39-7.34 (m, 3H), 4.72 (s, 2H), 1.26 (s, 9H). .sup.13C NMR (150 MHz, CDCl.sub.3) 173.92, 152.03, 132.13, 129.51, 128.40, 121.70, 101.73, 78.71, 70.52, 37.39, 28.06. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.16NO.sub.3.sup. [MH].sup.: 258.1136, found: 258.1132.
C(sp.SUP.3.)-H Iodination
(65) ##STR00048##
(66) General Procedures for the C(sp.sup.3)-H Iodination of UV Active Ketones: Substrate 1 (0.10 mmol), Pd(TFA).sub.2 (0.01 mmol, 3.3 mg), I.sub.2 (0.10 mmol, 25.4 mg) and Phl(OAc).sub.2 (0.10 mmol, 32.2 mg) were weighed into a reaction vial (10 mL) with a magnetic stir bar under air. 1,4-Dioxane (1.25 mL) was added, and the vial was sealed with a cap. The reaction mixture was stirred at 40 C. for 20 hours. Upon completion, the reaction mixture was cooled to room temperature and diluted with EtOAc. Then the reaction mixture was filtered through a plug of silicon gel and transferred to a reaction vial (10 mL) with a magnetic stir bar. The solvent was evaporated under vacuum. Anhydrous MeOH (0.5 mL) was added to the mixture. SOCl.sub.2 (0.30 mmol, 22 L) was added dropwise at room temperature. The vial was sealed with a cap. The reaction mixture was stirred at room temperature for 1 hour. Upon completion, the reaction mixture was cooled to room temperature and the solvent was removed under vacuum. The resulting mixture was purified by preparative thin-layer chromatography.
(67) ##STR00049##
(68) General Procedures for the C(sp.sup.3)-H Iodination of UV Inactive Ketones: Substrate 1 (0.10 mmol), Pd(TFA).sub.2 (0.01 mmol, 3.3 mg), 1.sub.2 (0.10 mmol, 25.4 mg) and Phl(OAc).sub.2 (0.10 mmol, 32.2 mg) were weighed into a reaction vial (10 mL) with a magnetic stir bar under air. 1,4-Dioxane (1.25 mL) was added, and the vial was sealed with a cap. The reaction mixture was stirred at 40 C. for 20 hours. Upon completion, the reaction mixture was cooled to room temperature and diluted with EtOAc. Then the reaction mixture was filtered through a plug of silicon gel and transferred to a reaction vial (10 mL) with a magnetic stir bar. The solvent was evaporated under vacuum. Anhydrous DCM (0.5 mL) and DMF (ca. 10 L) were added to the mixture. (COCl).sub.2 (0.15 mmol, 13 L) was added dropwise at room temperature. The vial was sealed with a cap. The reaction mixture was stirred at room temperature for 30 min before excess (COCl).sub.2 and solvent were evaporated. To the mixture was added anhydrous DCM (0.5 mL), followed by the dropwise addition of 3,5-dimethylaniline (0.2 mmol, 25 L) to the mixture at room temperature. The vial was sealed with a cap. The reaction mixture was stirred at room temperature for 30 min. Upon completion, the reaction mixture was diluted with EtOAc. Then the reaction mixture was filtered through a plug of celite and the solvent was removed under vacuum. The resulting mixture was purified by preparative thin-layer chromatography.
(69) ##STR00050##
(E)-N-(3,5-dimethylphenyl)-2-(((4-iodo-3,3-dimethylbutan-2-ylidene)amino)oxy)acetamide (2a-mono)
(70) Substrate 1a was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2a-mono was obtained as a colorless oil (14.1 mg, 35%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.86 (br s, 1H), 7.19 (s, 2H), 6.76 (s, 1H), 4.62 (s, 2H), 3.31 (s, 2H), 2.29 (s, 6H), 1.96 (s, 3H), 1.29 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 168.32, 163.16, 138.66, 136.98, 126.25, 117.88, 73.01, 41.14, 25.46, 21.34, 18.61, 10.85. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.24IN.sub.2O.sub.2.sup.+ [M+H].sup.+: 403.0877, found: 403.0873.
(71) ##STR00051##
(E)-N-(3,5-dimethylphenyl)-2-(((4-iodo-3-(iodomethyl)-3-methylbutan-2-ylidene)amino)oxy)acetamide (2a-di)
(72) Substrate 1a was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2a-di was obtained as a colorless oil (26.4 mg, 50%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.75 (br s, 1H), 7.19 (s, 2H), 6.76 (s, 1H), 4.65 (s, 2H), 3.46 (ABq, J=10.2 Hz, 4H), 2.29 (s, 6H), 2.02 (s, 3H), 1.41 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 167.87, 160.45, 138.67, 136.81, 126.34, 117.88, 73.21, 43.67, 23.74, 21.33, 15.46, 11.62. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.23I.sub.2N.sub.2O.sub.2.sup.+ [M+H].sup.+: 528.9843, found: 528.9849.
(73) ##STR00052##
(E)-N-(3,5-dimethylphenyl)-2-(((3-(iodomethyl)-3-methylpentan-2-ylidene)amino)oxy)acetamide (2b-mono)
(74) Substrate 1b was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2b-mono was obtained as a colorless oil (12.5 mg, 30%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.83 (br s, 1H), 7.18 (s, 2H), 6.76 (s, 1H), 4.63 (ABq, J=16.2 Hz, 2H), 3.31 (ABq, J=10.2 Hz, 2H), 2.29 (s, 6H), 1.93 (s, 3H), 1.76-1.70 (m, 1H), 1.56-1.51 (m, 1H), 1.20 (s, 3H), 0.83 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 168.33, 162.34, 138.68, 136.98, 126.24, 117.81, 73.05, 44.45, 30.46, 25.54, 22.63, 21.34, 17.88, 11.02, 9.38. HRMS (ESI-TOF) Calcd for C.sub.17H.sub.26IN.sub.2O.sub.2.sup.+ [M+H].sup.+: 417.1033, found: 417.1029.
(75) ##STR00053##
(E)-N-(3,5-dimethylphenyl)-2-(((4-iodo-3-(iodomethyl)-3-methylbutan-2-ylidene)amino)oxy)acetamide (2b-di)
(76) Substrate 1b was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2b-di was obtained as a colorless oil (29.0 mg, 55%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.72 (br s, 1H), 7.18 (s, 2H), 6.76 (s, 1H), 4.65 (s, 2H), 3.48 (ABq, J=10.8 Hz, 4H), 2.29 (s, 6H), 2.01 (s, 3H), 1.73 (q, J=7.2 Hz, 2H), 0.82 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 167.81, 159.63, 138.69, 136.78, 126.34, 117.80, 73.23, 46.91, 27.87, 21.33, 15.41, 11.84, 9.62. HRMS (ESI-TOF) Calcd for C.sub.17H.sub.25I.sub.2N.sub.2O.sub.2.sup.+ [M+H].sup.+: 543.0000, found: 543.0007.
(77) ##STR00054##
(E)-N-(3,5-dimethylphenyl)-2-(((1-(1-(iodomethyl)cyclohexyl)ethylidene)amino)oxy)acetamide (2c)
(78) Substrate 1c was iodinated following the general iodination procedure except the reaction time is 3 hours. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2c was obtained as a colorless oil (26.5 mg, 60%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.89 (br s, 1H), 7.20 (s, 2H), 6.75 (s, 1H), 4.64 (s, 2H), 3.29 (s, 2H), 2.29 (s, 6H), 2.02-1.99 (m, 2H), 1.91 (s, 3H), 1.53-1.31 (m, 8H). .sup.13C NMR (150 MHz, CDCl.sub.3) 168.46, 161.85, 138.60, 136.97, 126.21, 117.93, 73.04, 44.14, 33.77, 25.84, 22.49, 21.32, 18.20, 10.62. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.28IN.sub.2O.sub.2.sup.+ [M+H].sup.+: 443.1190, found: 443.1196.
(79) ##STR00055##
N-(3,5-dimethylphenyl)-2-(((E)-((1S,4R)-3-(iodomethyl)-1,3-dimethylbicyclo[2.2.1]heptan-2-ylidene)amino)oxy)acetamide (2d)
(80) Substrate 1d was iodinated following the general iodination procedure except the reaction time is 3 hours and the reaction time is 3 h. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2d was obtained as a colorless oil (19.1 mg, 42%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.84 (br s, 1H), 7.16 (s, 2H), 6.77 (s, 1H), 4.55 (s, 2H), 3.45 (ABq, J=10.2 Hz, 2H), 2.30 (s, 6H), 2.02-1.97 (m, 1H), 1.96-1.93 (m, 1H), 1.92-1.87 (m, 2H), 1.74-1.68 (m, 1H), 1.58-1.56 (m, 1H), 1.49-1.44 (m, 1H), 1.40 (s, 3H), 1.37 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 171.68, 168.39, 138.73, 137.07, 126.26, 117.65, 73.36, 54.54, 47.64, 45.62, 43.05, 32.19, 26.10, 23.06, 22.84, 21.39, 8.31. HRMS (ESI-TOF) Calcd for C.sub.20H.sub.28IN.sub.2O.sub.2.sup.+ [M+H].sup.+: 455.1190, found: 455.1195.
(81) ##STR00056##
(E)-methyl 2-(((3-benzyl-4-iodo-3-methylbutan-2-ylidene)amino)oxy)acetate (2e-mono)
(82) Substrate 1e was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2e-mono was obtained as a colorless oil (15.6 mg, 40%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.27 (m, 2H), 7.24-7.21 (m, 1H), 7.16-7.15 (m, 2H), 4.58 (s, 2H), 3.73 (s, 3H), 3.29 (ABq. J=10.2 Hz, 2H), 2.90 (ABq, J=13.8 Hz, 2H), 1.93 (s, 3H), 1.20 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.57, 160.68, 136.94, 130.24, 128.06, 126.61, 70.53, 51.79, 44.48, 43.28, 23.68, 17.84, 11.84. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.21INO.sub.3.sup.+ [M+H].sup.+: 390.0561, found: 390.0555.
(83) ##STR00057##
(E)-methyl 2-(((3-benzyl-4-iodo-3-(iodomethyl)butan-2-ylidene)amino)oxy)acetate (2e-di)
(84) Substrate 1e was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2e-di was obtained as a colorless oil (20.6 mg, 40%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.30-7.21 (m, 5H), 4.54 (s, 2H), 3.70 (s, 3H), 3.43 (ABq, J=10.2 Hz, 4H), 2.97 (s, 2H), 2.00 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.20, 157.66, 135.89, 129.72, 128.29, 127.13, 70.74, 51.85, 47.19, 40.04, 15.86, 12.64. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.20I.sub.2NO.sub.3.sup.+ [M+H].sup.+: 515.9527, found: 515.9532.
(85) ##STR00058##
(E)-methyl 2-(((3-benzyl-3-(iodomethyl)pentan-2-ylidene)amino)oxy)acetate (2f)
(86) Substrate 1f was iodinated following the general iodination procedure except the reaction time is 3 hours. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2f was obtained as a colorless oil (29.0 mg, 72%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.25 (m, 2H), 7.23-7.20 (m, 3H), 4.54 (ABq, J=16.2 Hz, 2H), 3.70 (s, 3H), 3.24 (ABq, J=11.4 Hz, 2H), 2.87 (ABq, J=14.4 Hz, 2H), 1.99 (s, 3H), 1.68-1.61 (m, 2H), 0.82 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.52, 159.60, 136.90, 129.96, 128.10, 126.57, 70.45, 51.74, 47.73, 40.23, 28.90, 16.00, 12.31, 8.33. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.23INO.sub.3.sup.+ [M+H].sup.+: 404.0717, found: 404.0721.
(87) ##STR00059##
(E)-methyl 2-(((3-ethyl-3-(iodomethyl)-5-phenylpentan-2-ylidene)amino)oxy)acetate (2g)
(88) Substrate 1g was iodinated following the general iodination procedure except the reaction time is 3 hours. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2g was obtained as a colorless oil (30.9 mg, 74%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.29-7.27 (m, 2H), 7.20-7.17 (m, 3H), 4.64 (s, 2H), 3.73 (s, 3H), 3.50 (ABqd, J.sub.1=1.2 Hz, J.sub.2=10.8 Hz, 2H), 2.47 (td, J.sub.1=4.8 Hz, J.sub.2=13.2 Hz, 1H), 2.28 (td, J.sub.1=4.8 Hz, J.sub.2=13.2 Hz, 1H), 1.94 (s, 3H), 1.93-1.88 (m, 1H), 1.76-1.70 (m, 1H), 1.69-1.64 (m, 1H), 1.58-1.52 (m, 1H), 0.74 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.54, 159.74, 141.87, 128.42, 128.33, 125.90, 70.40, 51.76, 46.42, 38.82, 30.16, 28.97, 15.11, 11.53, 7.75. HRMS (ESI-TOF) Calcd for C.sub.17H.sub.25INO.sub.3.sup.+ [M+H].sup.+: 418.0874, found: 418.0880.
(89) ##STR00060##
(E)-methyl 2-(((6-(4-iodo-2,5-dimethylphenoxy)-3-(iodomethyl)-3-methylhexan-2-ylidene)amino)oxy)acetate (2h-mono)
(90) Substrate 1h was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Toluene:EtOAc=100:1 as eluent), 2h-mono was obtained as a colorless oil (29.4 mg, 50%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.51 (s, 1H), 6.67 (s, 1H), 4.62 (s, 2H), 3.90-3.87 (m, 2H), 3.74 (s, 3H), 3.37 (ABq, J=10.8 Hz, 2H), 2.37 (s, 3H), 2.13 (s, 3H), 1.91 (s, 3H), 1.84-1.80 (m, 1H), 1.68-1.63 (m, 3H), 1.22 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.58, 160.35, 157.27, 139.97, 139.43, 126.41, 112.58, 89.04, 70.44, 67.63, 51.76, 43.22, 34.37, 27.96, 24.59, 23.97, 18.20, 15.32, 11.12. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.28I.sub.2NO.sub.4.sup.+ [M+H].sup.+: 588.0102, found: 588.0106.
(91) ##STR00061##
(E)-methyl 2-(((6-(4-iodo-2,5-dimethylphenoxy)-3,3-bis(iodomethyl)hexan-2-ylidene)amino)oxy)acetate (2h-di)
(92) Substrate 1h was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Toluene:EtOAc=100:1 as eluent), 2h-di was obtained as a colorless oil (21.4 mg, 30%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.51 (s, 1H), 6.67 (s, 1H), 4.64 (s, 2H), 3.89 (t, J=6.0 Hz, 2H), 3.74 (s, 3H), 3.51 (ABq, J=10.8 Hz, 4H), 2.36 (s, 3H), 2.13 (s, 3H), 1.97 (s, 3H), 1.86-1.83 (m, 2H), 1.66-1.62 (m, 2H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.30, 157.88, 157.12, 140.02, 139.48, 126.34, 112.48, 89.17, 70.62, 67.13, 51.84, 46.02, 31.95, 27.96, 25.19, 15.96, 15.38, 11.62. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.27I.sub.3NO.sub.4.sup.+ [M+H].sup.+: 713.9069, found: 713.9062.
(93) ##STR00062##
(E)-methyl 2-(((3-iodo-2-(iodomethyl)-2-methyl-1-phenylpropylidene)amino)oxy)acetate (2i-mono)
(94) Substrate 1i was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2i-mono was obtained as a colorless oil (11.3 mg, 30%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.43-7.40 (m, 2H), 7.38-7.35 (m, 1H), 7.25-7.23 (m, 2H), 4.55 (s, 2H), 3.75 (s, 3H), 3.36 (s, 2H), 1.28 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.52, 162.74, 132.95, 128.25, 128.08, 127.40, 70.63, 51.74, 40.74, 26.72, 19.84. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.19INO.sub.3.sup.+ [M+H].sup.+: 376.0404, found: 376.0400.
(95) ##STR00063##
(E)-methyl 2-(((3-iodo-2-(iodomethyl)-2-methyl-1-phenylpropylidene)amino)oxy)acetate (2i-di)
(96) Substrate 1i was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2i-di was obtained as a colorless oil (21.5 mg, 43%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.45-7.42 (m, 2H), 7.40-7.38 (m, 1H), 7.34-7.32 (m, 2H), 4.57 (s, 2H), 3.76 (s, 3H), 3.49 (ABq, J=10.8 Hz, 4H), 1.41 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.22, 159.30, 132.08, 128.79, 128.31, 127.38, 70.83, 51.87, 43.11, 24.88, 17.66. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.18I.sub.2NO.sub.3.sup.+ [M+H].sup.+: 501.9371, found: 501.9375.
(97) ##STR00064##
(E)-methyl 2-(((3-iodo-1-(4-methoxyphenyl)-2,2-dimethylpropylidene)amino)oxy)acetate (2j-mono)
(98) Substrate 1j was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2j-mono was obtained as a colorless oil (11.7 mg, 29%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.20-7.17 (m, 2H), 6.95-6.93 (m, 2H), 4.56 (s, 2H), 3.82 (s, 3H), 3.75 (s, 3H), 3.33 (s, 2H), 1.28 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.57, 162.62, 159.33, 128.76, 124.97, 113.58, 70.61, 55.15, 51.73, 40.92, 26.70, 20.02. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.21INO.sub.4.sup.+ [M+H].sup.+: 406.0510, found: 406.0515.
(99) ##STR00065##
(E)-methyl 2-(((3-iodo-2-(iodomethyl)-1-(4-methoxyphenyl)-2-methylpropylidene)amino)oxy)acetate (2j-di)
(100) Substrate 1j was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2j-di was obtained as a colorless oil (22.3 mg, 42%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.26 (m, 2H), 6.97-6.94 (m, 2H), 4.57 (s, 2H), 3.82 (s, 3H), 3.76 (s, 3H), 3.48 (ABq, J=10.8 Hz, 4H), 1.41 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.27, 159.72, 159.26, 128.79, 124.04, 113.76, 70.80, 55.18, 51.85, 43.30, 24.84, 17.79. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.20I.sub.2NO.sub.4.sup.+ [M+H].sup.+: 531.9476, found: 531.9471.
(101) ##STR00066##
(E)-methyl 2-(((4-iodo-3,3-dimethyl-1-phenylbutan-2-ylidene)amino)oxy)acetate (2k-mono)
(102) Substrate 1k was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=10:1 as eluent), 2k-mono was obtained as a colorless oil (9.7 mg, 25%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.30-7.27 (m, 4H), 7.22-7.18 (m, 1H), 4.66 (s, 2H), 3.82 (s, 2H), 3.78 (s, 3H), 3.34 (s, 2H), 1.18 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.56, 161.85, 136.30, 128.52, 128.47, 126.23, 70.58, 51.81, 40.89, 31.78, 26.69, 20.17. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.21INO.sub.3.sup.+ [M+H].sup.+: 390.0561, found: 390.0569.
(103) ##STR00067##
(E)-methyl 2-(((4-iodo-3-(iodomethyl)-3-methyl-1-phenylbutan-2-ylidene)amino)oxy)acetate (2k-di)
(104) Substrate 1k was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=10:1 as eluent), 2k-di was obtained as a colorless oil (25.8 mg, 50%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.30-7.29 (m, 4H), 7.24-7.20 (m, 1H), 4.70 (s, 2H), 3.85 (s, 2H), 3.79 (s, 3H), 3.45 (ABq, J=10.2 Hz, 4H), 1.28 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.24, 158.72, 135.61, 128.64, 126.56, 70.82, 51.92, 43.41, 32.11, 24.85, 17.74. HRMS (ESI-TOF) Calcd for C.sub.15H.sub.20I.sub.2NO.sub.3.sup.+ [M+H].sup.+: 515.9527, found: 515.9520.
(105) ##STR00068##
(E)-2-(((1-cyano-4-iodo-3,3-dimethylbutan-2-ylidene)amino)oxy)-N-(3,5-dimethylphenyl)acetamide (2l)
(106) Substrate 1l was iodinated following the general iodination procedure except the reaction temperature is 80 C. After purification by preparative thin-layer chromatography (Hexane: EtOAc=2:1 as eluent), 2l was obtained as a colorless oil (21.4 mg, 50%). .sup.1H NMR (600 MHz, CDCl.sub.3) 8.06 (br s, 1H), 7.28 (s, 2H), 6.76 (s, 1H), 4.81 (s, 2H), 3.35 (s, 2H), 3.29 (s, 2H), 2.29 (s, 6H), 1.36 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 166.71, 154.24, 138.61, 137.06, 126.33, 117.78, 115.38, 74.28, 41.36, 25.44, 21.36, 15.99, 14.26. HRMS (ESI-TOF) Calcd for C.sub.17H.sub.23IN.sub.3O.sub.2.sup.+ [M+H].sup.+: 428.0829, found: 428.0822.
(107) ##STR00069##
(E)-ethyl 3-((2-((3,5-dimethylphenyl)amino)-2-oxoethoxy)imino)-5-iodo-4,4-dimethylpentanoate (2m-mono)
(108) Substrate 1m was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), the iodinated products were obtained as 3.4:1 (mono:di) inseparable mixtures (2m-mono, 26.1 mg, 55%). .sup.1H NMR (600 MHz, CDCl.sub.3) 8.63 (br s, 1H), 7.40 (s, 2H), 6.75 (s, 1H), 4.68 (s, 2H), 4.24 (q, J=7.2 Hz, 2H), 3.42 (s, 2H), 3.31 (s, 2H), 2.30 (s, 6H), 1.30 (t, J=7.2 Hz, 3H), 1.28 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 169.29, 168.21, 157.74, 138.34, 137.86, 125.83, 117.73, 73.51, 61.83, 40.63, 31.77, 25.58, 21.43, 17.59, 14.04. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.28IN.sub.2O.sub.4.sup.+ [M+H].sup.+: 475.1088, found: 475.1084.
(109) ##STR00070##
(E)-ethyl 3-((2-((3,5-dimethylphenyl)amino)-2-oxoethoxy)imino)-5-iodo-4-(iodomethyl)-4-methylpentanoate (2m-di)
(110) Substrate 1m was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), the iodinated products were obtained as 3.4:1 (mono:di) inseparable mixtures (2m-di, 10.2 mg, 17%). .sup.1H NMR (600 MHz, CDCl.sub.3) 8.60 (br s, 1H), 7.40 (s, 2H), 6.75 (s, 1H), 4.71 (s, 2H), 4.25 (q, J=7.2 Hz, 2H), 3.47 (s, 2H), 3.46 (ABq, J=10.8 Hz, 4H), 2.30 (s, 6H), 1.42 (s, 3H), 1.31 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 168.80, 167.79, 154.89, 138.36, 137.76, 125.91, 117.72, 73.80, 62.06, 43.30, 32.34, 29.44, 24.00, 17.60, 15.43. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.27I.sub.2N.sub.2O.sub.4.sup.+ [M+H].sup.+: 601.0055, found: 601.0051.
(111) ##STR00071##
(E)-ethyl 3-((2-((3,5-dimethylphenyl)amino)-2-oxoethoxy)imino)-2-(iodomethyl)-2-methylbutanoate (2n-mono)
(112) Substrate 1n was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), the iodinated products were obtained as 4.0:1 (mono:di) inseparable mixtures (2n-mono, 24.8 mg, 54%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.75 (br s, 1H), 7.18 (s, 2H), 6.77 (s, 1H), 4.66 (ABq, J=16.2 Hz, 2H), 4.28-4.17 (m, 2H), 3.59 (ABq, J=10.2 Hz, 2H), 2.30 (s, 6H), 1.97 (s, 3H), 1.50 (s, 3H), 1.27 (t, J=7.2 Hz, 3H). .sup.13C NMR of mixture (150 MHz, CDCl.sub.3) 170.70, 167.78, 167.42, 167.16, 158.93, 156.69, 138.71, 138.70, 136.87, 136.72, 126.43, 126.34, 117.83, 117.76, 73.49, 73.27, 62.96, 62.05, 56.71, 53.06, 22.05, 21.32, 14.12, 14.08, 12.74, 12.64, 11.48, 10.59. HRMS (ESI-TOF) Calcd for C.sub.18H.sub.26IN.sub.2O.sub.4.sup.+ [M+H].sup.+: 461.0932, found: 461.0939.
(113) ##STR00072##
(E)-ethyl 3-((2-((3,5-dimethylphenyl)amino)-2-oxoethoxy)imino)-2,2-bis(iodomethyl)butanoate (2n-di)
(114) Substrate 1n was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), the iodinated products were obtained as 4.0:1 (mono:di) inseparable mixtures (2n-di, 8.2 mg, 14%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.68 (br s, 1H), 7.18 (s, 2H), 6.77 (s, 1H), 4.70 (s, 2H), 4.28-4.17 (m, 2H), 3.78 (ABq, J=9.6 Hz, 4H), 2.29 (s, 6H), 1.98 (s, 3H), 1.31 (t, J=7.2 Hz, 3H). .sup.13C NMR of mixture (150 MHz, CDCl.sub.3) 170.70, 167.78, 167.42, 167.16, 158.93, 156.69, 138.71, 138.70, 136.87, 136.72, 126.43, 126.34, 117.83, 117.76, 73.49, 73.27, 62.96, 62.05, 56.71, 53.06, 22.05, 21.32, 14.12, 14.08, 12.74, 12.64, 11.48, 10.59. HRMS (ESI-TOF) Calcd for C.sub.18H.sub.25I.sub.2N.sub.2O.sub.4.sup.+ [M+H].sup.+: 586.9898, found: 586.9891.
(115) ##STR00073##
(E)-ethyl 2-benzyl-2-(iodomethyl)-3-((2-methoxy-2-oxoethoxy)imino)butanoate (2o)
(116) Substrate 1o was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2o was obtained as 1.6:1 (2o: starting material) inseparable mixture (32.2 mg, 60%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.28-7.18 (m, 4H), 7.11-7.09 (m, 1H), 4.57 (ABq, J=16.2 Hz, 2H), 4.27-4.18 (m, 2H), 3.73 (s, 3H), 3.41 (ABq, J=11.4 Hz, 2H), 3.28 (ABq, J=14.4 Hz, 2H), 1.93 (s, 3H), 1.28 (t, J=7.2 Hz, 3H). .sup.13C NMR of mixture (150 MHz, CDCl.sub.3) 173.68, 170.47, 170.17, 170.13, 156.45, 136.99, 135.64, 130.42, 130.04, 128.26, 128.23, 127.94, 127.02, 126.53, 70.74, 70.52, 61.94, 61.06, 57.50, 53.74, 51.82, 51.73, 41.10, 37.69, 20.25, 14.07, 14.03, 13.26, 13.13, 9.90. HRMS (ESI-TOF) Calcd for C.sub.24H.sub.30IN.sub.2O.sub.4.sup.+ [M+H].sup.+: 537.1245, found: 537.1240.
(117) ##STR00074##
(E)-methyl 6-(iodomethyl)-6,8,8,9,9-pentamethyl-5-phenyl-3,7-dioxa-4-aza-8-siladec-4-en-1-oate (2p-mono)
(118) Substrate 1p was iodinated following the general iodination procedure except the reaction temperature is 80 C. After purification by preparative thin-layer chromatography (Toluene:EtOAc=100:1 as eluent), 2p-mono was obtained as a colorless oil (22.1 mg, 45%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.40-7.34 (m, 5H), 4.58 (s, 2H), 3.76 (s, 3H), 3.42 (ABq, J=9.6 Hz, 2H), 1.68 (s, 3H), 0.80 (s, 9H), 0.14 (s, 3H), 0.01 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.42, 161.17, 131.92, 128.45, 128.22, 127.78, 76.40, 70.82, 51.81, 27.11, 25.89, 18.37, 17.86, 1.80, 2.48. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.31INO.sub.4Si.sup.+ [M+H].sup.+: 492.1062, found: 492.1066.
(119) ##STR00075##
(E)-methyl 6,6-bis(iodomethyl)-8,8,9,9-tetramethyl-5-phenyl-3,7-dioxa-4-aza-8-siladec-4-en-1-oate (2p-di)
(120) Substrate 1p was iodinated following the general iodination procedure except the reaction temperature is 80 C. After purification by preparative thin-layer chromatography (Toluene:EtOAc=100:1 as eluent), 2p-di was obtained as a colorless oil (12.3 mg, 20%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.46-7.44 (m, 2H), 7.42-7.38 (m, 3H), 4.63 (s, 2H), 3.78 (s, 3H), 3.69 (ABq, J=10.2 Hz, 4H), 0.92 (s, 9H), 0.15 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.05, 156.26, 130.90, 129.13, 128.42, 128.02, 76.21, 71.10, 51.98, 26.02, 18.68, 15.86, 2.14. HRMS (ESI-TOF) Calcd for C.sub.19H.sub.30I.sub.2NO.sub.4Si.sup.+ [M+H].sup.+: 618.0028, found: 618.0020.
(121) ##STR00076##
methyl 2-(((E)-((E)-5-iodo-4,4-dimethyl-1-phenylpent-1-en-3-ylidene)amino)oxy)acetate (2q-mono)
(122) Substrate 1q was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:Acetone=20:1 as eluent), 2q-mono was obtained as a colorless oil (14.0 mg, 35%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.49-7.46 (m, 2H), 7.42 (d, J=16.8 Hz, 1H), 7.37-7.34 (m, 2H), 7.32-7.29 (m, 1H), 6.56 (d, J=16.8 Hz, 1H), 4.68 (s, 2H), 3.78 (s, 3H), 3.41 (s, 2H), 1.36 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.43, 158.24, 139.42, 136.52, 128.80, 128.69, 126.99, 116.05, 71.00, 51.86, 40.72, 26.84, 20.24. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.21INO.sub.3.sup.+ [M+H].sup.+: 402.0561, found: 402.0555.
(123) ##STR00077##
methyl 2-(((E)-((E)-5-iodo-4-(iodomethyl)-4-methyl-1-phenylpent-1-en-3-ylidene)amino)oxy)acetate (2q-di)
(124) Substrate 1q was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=20:1 as eluent), 2q-di was obtained as a colorless oil (18.4 mg, 35%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.49-7.47 (m, 2H), 7.42 (d, J=16.8 Hz, 1H), 7.38-7.36 (m, 2H), 7.33-7.31 (m, 1H), 6.49 (d, J=16.8 Hz, 1H), 4.69 (s, 2H), 3.79 (s, 3H), 3.55 (ABq, J=10.2 Hz, 4H), 1.52 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 170.16, 155.74, 140.17, 136.13, 129.06, 128.74, 127.08, 115.43, 71.17, 51.96, 43.13, 24.92, 17.60. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.20I.sub.2NO.sub.3.sup.+ [M+H].sup.+: 527.9527, found: 527.9521.
(125) ##STR00078##
(E)-methyl 2-(((5-iodo-4,4-dimethyl-1-phenylpent-1-yn-3-ylidene)amino)oxy)acetate (2r-mono)
(126) Substrate 1r was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=10:1 as eluent), the iodinated products were obtained as 1.9:1 (mono:di) inseparable mixtures (2r-mono, 20.7 mg, 52%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.55-7.53 (m, 2H), 7.38-7.34 (m, 3H), 4.73 (s, 2H), 3.78 (s, 3H), 3.45 (s, 2H), 1.39 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 169.70, 146.92, 132.15, 129.59, 128.40, 121.55, 101.62, 78.23, 71.19, 51.92, 40.46, 26.18, 16.11. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.19INO.sub.3.sup.+ [M+H].sup.+: 400.0404, found: 400.0400.
(127) ##STR00079##
(E)-methyl 2-(((3-iodo-2-(iodomethyl)-2-methyl-1-phenylpropylidene)amino)oxy)acetate (2r-di)
(128) Substrate 1r was iodinated following the general iodination procedure. After purification by preparative thin-layer chromatography (Hexane:EtOAc=10:1 as eluent), the iodinated products were obtained as 1.9:1 (mono:di) inseparable mixtures (2r-di, 8.4 mg, 16%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.56-7.54 (m, 2H), 7.43-7.39 (m, 3H), 4.75 (s, 2H), 3.79 (s, 3H), 3.59 (ABq, J=10.2 Hz, 4H), 1.54 (s, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 169.96, 143.74, 132.21, 129.87, 128.47, 121.15, 102.03, 77.69, 71.39, 52.02, 42.89, 24.71, 18.97. HRMS (ESI-TOF) Calcd for C.sub.16H.sub.18I.sub.2NO.sub.3.sup.+ [M+H].sup.+: 525.9371, found: 525.9377.
(129) The Synthesis and Characterization of Palladacycle
(130) ##STR00080##
(131) The General Procedures for the Palladacycle Synthesis: Substrate 1a (0.1 mmol, 17.3 mg) and Pd(OAc).sub.2 (0.12 mmol, 27.0 mg) were weighed into a reaction vial (10 mL) with a magnetic stir bar under air. HFIP (1.0 mL) was added, and the vial was sealed with a cap. The reaction mixture was stirred at 80 C. for 12 hours. Upon completion, the reaction mixture was cooled to room temperature and PPh.sub.3 (0.12 mmol, 31.4 mg) was added. The reaction was stirred for another 1 h at 80 C. Upon completion, the reaction mixture was cooled to room temperature and diluted with EtOAc. Then the reaction mixture was filtered through a plug of celite. The solvent was removed under vacuum and the resulting mixture was purified by preparative thin-layer chromatography with EtOAc:MeOH=10:1 as the eluent.
(132) ##STR00081##
(133) Palladacycle (3)
(134) Substrate 1a was palladated following the general procedures. After purification by preparative thin-layer chromatography (EtOAc:MeOH=10:1 as eluent), 3 was obtained as a white solid (43.7 mg, 81%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.60-7.56 (m, 6H), 7.46-7.39 (m, 9H), 4.57 (s, 2H), 1.95 (s, 3H), 1.57 (d, J=3.6 Hz, 2H), 1.11 (s, 6H). .sup.13C NMR (150 MHz, CDCl.sub.3) 178.99, 172.54, 134.04 (d, J=12.0 Hz), 130.60, 128.57, 128.49, 76.00, 50.26, 40.35, 28.65, 12.24. HRMS (ESI-TOF) Calcd for C.sub.26H.sub.28NO.sub.3PPd [M+H].sup.+: 539.0842, found: 539.0850.
(135) The Removal of Auxiliary
(136) ##STR00082##
(137) The removal of auxiliary: 2g (0.05 mmol, 20.9 mg) was weighed into a reaction vial (10 mL) with a magnetic stir bar under air. 0.5 mL of conc. HCl 4 M in dioxane was added, and the vial was sealed with a cap. The reaction mixture was stirred at 100 C. for 2 hours. Upon completion, the reaction mixture was cooled to room temperature and the solvent was removed under vacuum. The resulting mixture was purified by preparative thin-layer chromatography by using toluene/EtOAc (100:1) as the eluent to give 11.6 mg of 2g-Ketone (70% yield).
(138) ##STR00083##
3-ethyl-3-(iodomethyl)-5-phenylpentan-2-one (2g-Ketone)
(139) Colorless oil (11.6 mg, 70%). .sup.1H NMR (600 MHz, CDCl.sub.3) 7.30-7.28 (m, 2H), 7.22-7.17 (m, 3H), 3.50 (q, J=10.8 Hz, 2H), 2.51-2.46 (m, 1H), 2.30-2.26 (m, 1H), 2.23 (s, 3H), 2.04-1.98 (m, 1H), 1.96-1.90 (m, 1H), 1.82-1.73 (m, 2H), 0.80 (t, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) 209.25, 141.20, 128.55, 128.26, 126.19, 54.41, 38.04, 30.41, 28.63, 26.02, 12.15, 8.24. HRMS (ESI-TOF) Calcd for C.sub.14H.sub.20IO.sup.+ [M+H].sup.+: 331.0553, found: 331.0560.
(140) General Procedures for the C(sp.sup.3)-H Arylation of Ketones: Substrate 1 (0.10 mmol, 18.7 mg), Arl (0.20 mmol, 52.4 mg for methyl p-iodobenzoate), Pd(OAc).sub.2 (0.01 mmol, 2.3 mg), and AgTFA (0.20 mmol, 44.2 mg) were weighed into a reaction vial (10 mL) with a magnetic stir bar under air. HFIP (1.0 mL) was added, and the vial was sealed with a cap. The reaction mixture was stirred at 120 C. for 20 hours. Upon completion, the reaction mixture was cooled to room temperature and diluted with EtOAc. Then the reaction mixture was filtered through a plug of silicon gel and transferred to a reaction vial (10 mL) with a magnetic stir bar. The solvent was evaporated under vacuum. Anhydrous MeOH (1.0 mL) was added to the mixture. SOCl.sub.2 (0.30 mmol, 22 L) was added dropwise at room temperature. The vial was sealed with a cap. The reaction mixture was stirred at room temperature for 1 hour. Upon completion, the reaction mixture was cooled to room temperature and the solvent was removed under vacuum. The resulting mixture was purified by preparative thin-layer chromatography.
(141) ##STR00084##
Methyl 4-(4-(((1-methoxy-2-methyl-1-oxopropan-2-yl)oxy)imino)pentan-2-yl)benzoate (2)
(142) Substrate 1 was arylated following the general arylation procedure using methyl p-iodobenzoate as Arl. After purification by preparative thin-layer chromatography (Hexane:EtOAc=5:1 as eluent), 2 was obtained as E/Z (3.7:1) mixture (25.1 mg, 75%). .sup.1H NMR (600 MHz, CDCl.sub.3) of E isomer (major) 7.96-7.94 (m, 2H), 7.27-7.25 (m, 2H), 3.90 (s, 3H), 3.67 (s, 3H), 3.10 (sextet, J=7.2 Hz, 1H), 2.44 (ABqd, J.sub.1=7.2 Hz, J.sub.2=14.4 Hz, 2H), 1.79 (s, 3H), 1.42 (s, 3H), 1.39 (s, 3H), 1.24 (d, J=6.6 Hz, 3H). .sup.1H NMR (600 MHz, CDCl.sub.3) of Z isomer (minor) 7.98-7.96 (m, 2H), 7.32-7.30 (m, 2H), 3.90 (s, 3H), 3.72 (s, 3H), 3.27 (sextet, J=7.2 Hz, 1H), 2.60 (ABqd, J.sub.1=7.2 Hz, J.sub.2=13.2 Hz, 2H), 1.62 (s, 3H), 1.49 (s, 3H), 1.44 (s, 3H), 1.30 (d, J=7.2 Hz, 3H). .sup.13C NMR (150 MHz, CDCl.sub.3) of E/Z mixture 174.95, 174.92, 167.06, 156.49, 155.99, 151.95, 151.76, 129.74, 129.73, 128.07, 126.99, 126.96, 80.68, 51.95, 43.80, 37.91, 37.01, 36.79, 24.30, 24.17, 24.06, 24.03, 21.76, 21.52, 20.84, 14.50. HRMS (ESI-TOF) Calcd for C.sub.18H.sub.26NO.sub.5.sup. [MH].sup.: 336.1805, found: 336.1800.
DOCUMENTS CITED IN EXAMPLES
(143) (1) (a) Peter, M.; Gleiter, R.; Rominger, F.; Oeser, T. Eur. J. Org. Chem. 2004, 3212. (b) Maruyama, K.; Noguchi-Yachide, T.; Sugita, K.; Hashimoto, Y.; Ishikawa, M. Bioorg. Med. Chem. Lett. 2010, 20, 6661. (2) Yang, Q.-L.; Li, Y.-Q.; Ma, C.; Fang, P.; Zhang, X.-J.; Mei, T.-S. J. Am. Chem. Soc. 2017, 139, 3293. (3) Ushijima, S.; Dohi, S.; Moriyama, K.; Togo, H. Tetrahedron, 2012, 68, 1436. (4) Ohkuma, T.; Sandoval, C. A.; Srinivasan, R.; Lin, Q.; Wei, Y.; Muniz, K.; Noyori, R. J. Am. Chem. Soc. 2005, 127, 8288. (5) Li, X.; Li, L.; Tang, Y.; Zhong, L.; Cun, L.; Zhu, J.; Liao, J.; Deng, J. J. Org. Chem. 2010, 75, 2981. (6) Yin, W.; He, H.; Zhang, Y.; Luo, D.; He, H. Synthesis 2014, 46, 2617.
(144) All patents and publications referred to herein are incorporated by reference herein to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference in its entirety.
(145) The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.