The present disclosure provides a method for efficiently producing and providing compounds having a spirooxindole skeleton, for example compounds having a spirooxindole skeleton and having antitumor activity that inhibit the interaction between Mdm2 protein and p53 protein, or intermediates thereof, using an asymmetric catalyst. Compounds having optically active tricyclic dispiroindole skeletons are obtained through catalytic asymmetric 1,3-dipolar cycloaddition reaction using ketimine as a reaction substrate and using a chiral ligand and a Lewis acid.

A highly efficient, Z-selective ring-closing metathesis system for the formation of macrocycles using a stereoretentive, ruthenium-based catalyst supported by a dithiolate ligand is reported. This catalyst is demonstrated to be remarkably active as observed in initiation experiments showing complete catalyst initiation at 20 C. within 10 min. Using easily accessible diene starting materials bearing a Z-olefin moiety, macrocyclization reactions generated products with significantly higher Z-selectivity in appreciably shorter reaction times, in higher yield, and with much lower catalyst loadings than in previously reported systems. Macrocyclic lactones ranging in size from twelve-membered to seventeen-membered rings are synthesized in moderate to high yields (68-79% yield) with excellent Z-selectivity (95%-99% Z).

Markovnikov-selective palladium catalyst for carbonylation of alkynes is formed from a bisphosphite having formula (1): ##STR00001## The carbonylation catalyst is suited for the preparation of a branched heteroarene-keto product from an alkyne substrate, CO and heterocycle in high yields with low amounts of the linear product.

The present disclosure provides a method for efficiently producing and providing compounds having a spirooxindole skeleton, for example compounds having a spirooxindole skeleton and having antitumor activity that inhibit the interaction between Mdm2 protein and p53 protein, or intermediates thereof, using an asymmetric catalyst. Compounds having optically active tricyclic dispiroindole skeletons are obtained through catalytic asymmetric 1,3-dipolar cycloaddition reaction using ketimine as a reaction substrate and using a chiral ligand and a Lewis acid.

Process for methoxycarbonylation with formic acid and methanol.

The invention relates to the use of ruthenium complexes, which are homogeneous catalysts and/or precatalysts of the olefin metathesis reaction, which lead to the production of alkenes containing an internal (non-terminal) double CC bond.

##STR00001##

Provided herein are metal organic frameworks comprising metal nodes and N-donor organic ligands. Methods for capturing chemical species from fluid compositions comprise contacting a metal organic framework characterized by the formula [M.sub.aM.sub.bF.sub.6-n(O/H.sub.2O).sub.w(Ligand).sub.x(solvent).sub.y].sub.z with a fluid composition and capturing one or more chemical species from the fluid composition.

The present invention relates to single thread composite fibers comprising at least one binder and at least one active catalyst for the capture and degradation of chemical threats such as chemical warfare agents (CWA), biological warfare agents, and toxic industrial chemicals (TIC) and a method for producing the same. The invention fibers are applicable to the fields of protective garments, filtration materials, and decontamination materials.

A method for manufacturing a modified porous organic framework includes steps as follows. A mixed solution is provided. The mixed solution includes a porous organic framework, a plurality of group donors and a solvent. The porous organic framework includes a plurality of first ligands. Each of the first ligands includes at least one tetrazine group. Each of the group donors includes a reactive group and a modifying group covalently connected with each other. The reactive groups are alkenyl groups, alkynyl groups, aldehyde groups, ketone groups or a combination thereof. A modifying step is conducted, wherein at least one of the reactive groups of the group donors is reacted with at least one of the tetrazine groups of the first ligands, so that at least one of the modifying groups of the group donors is covalently connected with the porous organic framework, whereby the modified porous organic framework is obtained.

A process for producing alpha-olefin dimers comprises contacting, at a temperature of 80 C. or more, a feedstock comprising at least one C.sub.8+ (linear) alpha-olefin with a catalyst system comprising activator and one or more catalyst compounds represented by the formula: ##STR00001##
where M is a Group 4 metal; n is 1, 2, or 3; R.sup.A is hydrogen or a C.sub.1 to C.sub.10 alkyl; each of R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, and R.sup.8 is independently selected from hydrogen and C.sub.1 to C.sub.10 alkyl; each X is independently selected from the group consisting of hydrocarbyl radicals having from 1 to 20 carbon atoms, hydrides, amides, alkoxides, sulfides, phosphides, halides, and a combination thereof, (two X's may form a part of a fused ring or a ring system), the contacting being conducted under conditions effective to oligomerize at least part of C.sub.8+ alpha-olefin to produce an oligomerized product containing at least 30 wt % of the alpha-olefin dimer and at least 80 mol % of vinylidene unsaturation, where the conversion of the alpha olefin is at least 10 wt %, based upon the weight of the alpha olefin monomer entering the reactor and the weight of dimer produced.