Patent classifications
C07B2200/09
MODIFIED USY ZEOLITIC CATALYST FOR ISOMERIZATION OF ALKYLATED AROMATICS, AND METHOD FOR ISOMERIZATION OF ALKYLATED AROMATICS
The present invention relates to a catalyst for isomerization of alkylated aromatics such as mixed xylenes, using xylene isomerization catalyst particles including post-framework modified USY zeolite in which zirconium atoms and/or titanium atoms and/or hafnium atoms form a part of a framework of an ultra-stable Y-type zeolite.
METHOD FOR PRODUCING DIFLUOROETHYLENE
Provided is a method for obtaining HFO-1132(E) and/or HFO-1132(Z) efficiently. The method is a method for producing HFO-1132(E) and/or HFO-1132(Z), comprising supplying a composition containing HFO-1132(E) and/or HFO-1132(Z) to a reactor, and performing an isomerization reaction between HFO-1132(E) and HFO-1132(Z).
Fluoroolefin production method
The present disclosure provides a method for producing fluoroolefin represented by formula (1): CX.sup.1X.sup.2═CX.sup.3X.sup.4, wherein X.sup.1, X.sup.2, X.sup.3, and X.sup.4 are the same or different, and represent a hydrogen atom or a fluorine atom, with high selectivity. Specifically, the present disclosure is a method for producing fluoroolefin represented by formula (1), wherein the method includes the step of performing dehydrofluorination by bringing a fluorocarbon represented by formula (2): CX.sup.1X.sup.2FCX.sup.3X.sup.4H, wherein X.sup.1, X.sup.2, X.sup.3, and X.sup.4 are as defined above, into contact with a base, and the dehydrofluorination step is performed in the liquid phase at a temperature of −70° C. or higher to less than 120° C.
METHOD FOR THE STEREOISOMERIZATION OF CHIRAL COMPOUNDS
The present invention provides a novel method for the controlled stereoisomerization (comprising the stereo-conversion of chiral compounds to racemates, non-racemic mixtures and mixtures of epimers). The method of the invention provides the fully controlled generation of mixtures of different ratios of (S) and (R) stereoisomers, both enantiomers and diastereomers, of a given compound or a mixture of compounds. Such mixtures and isotopically labeled variants of said mixtures provided by the present invention are useful as an authenticity or external or internal standards in various biochemical and medical applications. Further, with the method of the invention it is possible to generate specific stereoisomers from some amino acids as well as degradation and oxidation products thereof which were previously not available. Thence, the invention provides in additional aspects the generation of a group of previously unavailable stereoisomers (enantiomers, epimers, and mixtures thereof such as a racemate) with amino acid type structures.
(Z)-SOLANONE, AND PREPARATION PROCESS AND USE THEREOF
A (Z)-solanone has the steric formula of:
##STR00001##
with the name of (S,Z)-5-isopropyl-8-methyl-6,8-diene-2-one or (R,Z)-5-isopropyl-8-methyl-6,8-diene-2-one. A process for the preparation of the (Z)-type solanone and the use thereof in flavoring of cigarette shred are further disclosed. The process includes the following steps: (1) reacting isopentanal and methyl vinyl ketone, under the action of a catalyst and a co-catalyst, to give (S)-2-isopropyl-5-carbonylhexanal or (R)-2-isopropyl-5-carbonylhexanal; (2) reacting the (S)-2-isopropyl-5-carbonylhexanal or the (R)-2-isopropyl-5-carbonylhexanal obtained in step (1) with (iodomethyl)triphenylphosphonium iodide, to give (S,Z)-7-iodo-5-isopropyl-6-ene-2-one or (R,Z)-7-iodo-5-isopropyl-6-ene-2-one; and (3) reacting the (S,Z)-7-iodo-5-isopropyl-6-ene-2-one or the (R,Z)-7-iodo-5-isopropyl-6-ene-2-one obtained in step (2) with pinacol isopropenylborate in the presence of a catalyst to give the (Z)-solanone.
Process for the preparation of unsaturated carboxylic acids by carbonylation of allyl alcohols and their acylation products
The present invention relates to a process for carbonylating allyl alcohols at low temperature, low pressure and/or low catalyst loading. In an alternative embodiment, an acylation product of the allyl alcohol is used for the carbonylation. The present invention likewise relates to the preparation of conversion products of these carbonylation products and specifically of (−)-ambrox.
ENERGY SOURCE SUPPLY SYSTEMS, ENERGY SOURCE SUPPLY DEVICES, AND RELATED METHODS
Some embodiments include an appliance energy source supply system for an energy source supply appliance. The appliance energy source supply system can comprise a first thermal control device and a second thermal control device. The appliance energy source supply system can be configured so that a hydrogen fuel energy source is selectively received by one of the first thermal control device or the second thermal control device before the hydrogen fuel energy source is made available to a receiver vehicle. Other embodiments of related systems, devices, and methods also are provided.
SULFOXIMINE GLYCOSIDASE INHIBITORS
Compounds of formula (I), wherein A, R, W, Q, n, and m have the meaning according to the claims, can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.
##STR00001##
RIGIDIFIED PENTADENTATE CHELATING AGENTS USEFUL FOR THE [AL18F]2+ LABELLING OF BIOMOLECULES
Rigidified pentadentate chelating agents of Formulae (I) and (II), which are useful for the [Al.sup.18F].sup.2+ labelling of biomolecules are provided. The rigidified pentadentate chelating agents are used to form coordination complexes with [Al.sup.18F].sup.2+, which are particularly advantageous for use as tracers in molecular imaging techniques.
##STR00001##
Process for synthesizing fluorinated cyclic aliphatic compounds
The present invention relates to a novel method for producing fluorinated cycloaliphatic compounds from the analogous aromatic compounds by hydrogenation with an Rh-carbene catalyst system.