专利号:US-8921580-B2 优先权日:2012-05-09 标 题 :Methods and systems for the formation of cyclic carbonates 发明人:HATTON TREVOR ALAN; JAMISON TIMOTHY F; KOZAK JENNIFER AIDEN; SIMEON FRITZ; WU JIE 权利人:MASSACHUSETTS INST TECHNOLOGY 摘要:Described herein are inventive methods for synthesis of cyclic carbonates from CO 2 and epoxide. In some embodiments, the methods are carried out in the presence of a catalyst comprising an electrophilic halogen. In some embodiments, the methods are carried out in a flow reactor.
专利号:US-2009182016-A1 优先权日:2006-05-23 标题 :Optical enantiomers of phenyramidol and process for chiral synthesis 发明人:DATLA ANUPAMA; WALAVALKER PRAMOD ABAJI; KONDA ASHOK; TRIVIKRAM SREENATH BABUNATH 权利人:DATLA ANUPAMA; WALAVALKER PRAMOD ABAJI; KONDA ASHOK; TRIVIKRAM SREENATH BABUNATH 摘要:The present invention discloses optically pure (R) and (S) Phenyramidol enantiomers and their pharmaceutically acceptable salts, a process for synthesising such enantiomers by means of a styrene oxide based asymmetric synthesis, and also a clinical evaluation of (R) and (S) enantiomers of Phenyramidol, their salts and compositions thereof for enhanced/newer therapeutic benefits.
专利号:US-8389551-B2 优先权日:2006-05-23 标题:Optical enantiomers of phenyramidol and process for chiral synthesis 发明人:DATLA ANUPAMA; WALAVALKER PRAMOD ABAJI; KONDA ASHOK; TRIVIKRAM SREENATH BABUNATH 权利人:DATLA ANUPAMA; WALAVALKER PRAMOD ABAJI; KONDA ASHOK; TRIVIKRAM SREENATH BABUNATH; FERMENTA BIOTECH UK LTD 摘要:The present invention discloses optically pure (R) and (S) Phenyramidol enantiomers and their pharmaceutically acceptable salts, a process for synthesizing such enantiomers by means of a styrene oxide based synthesis, and also a clinical evaluation of (R) and (S) enantiomers of Phenyramidol, their salts and compositions thereof for enhanced/newer therapeutic benefits.
专利号:US-7220870-B2 优先权日:1995-03-14 标 题:Hydrolytic kinetic resolution of cyclic substrates 发明人:JACOBSEN ERIC N; TOKUNAGA MAKOTO; LARROW JAY F 权利人:HARVARD COLLEGE 摘要:The present invention relates to a process for stereoselective or regioselective chemical synthesis which generally comprises reacting a nucleophile and a chiral or prochiral cyclic substrate in the presence of a non-racemic, chiral catalyst to produce a stereoisomerically- and/or regioisomerically-enriched product. The present invention also relates to hydrolytic kinetic resolutions of racemic and diastereomeric mixtures of epoxides.
专利号:WO-2006003790-A1 优先权日:2004-06-30 标 题:Reaction apparatus for hydrophobic compound and method of reaction therewith 发明人:NODA KENICHI; IRISA SHIRO; KOGURE TOMONARI; SAKATA MINORU; TOKIDA AKIHIKO 权利人:BUSSAN NANOTECH RES INST INC; NODA KENICHI; IRISA SHIRO; KOGURE TOMONARI; SAKATA MINORU; TOKIDA AKIHIKO 摘要:A reaction apparatus for hydrophobic compound for carrying out reaction of hydrophobic compounds with the use of a biocatalyst, characterized by having a microchannel chip comprising a first channel for circulation of a hydrophobic liquid material containing a hydrophobic compound, a second channel for circulation of a water base liquid material containing a biocatalyst and a third channel for circulation of the hydrophobic liquid material and water base liquid material which is connected to the first channel and second channel. By virtue of this reaction apparatus, the reaction efficiency of hydrophobic compound can be satisfactorily enhanced in a wide variety of reactions conducted in the presence of a biocatalyst. Accordingly, the provided reaction apparatus for hydrophobic compound and method of reaction therewith are applicable to, being important in organic chemistry, a hydrolysis reaction, redox reaction, transition reaction, substitution reaction, elimination reaction, condensation reaction, addition reaction, isomerization reaction, asymmetric synthesis reaction, etc., and future progress is promising in the field of biocatalytic reaction for hydrophobic compounds.
专利号:WO-2025103462-A1 优先权日:2023-11-17 标题:Substituted 2, 3-dihydrobenzo [d] [1, 3] oxaphosphole ligand, preparation method and use thereof 发明人:CHEN GENQIANG; ZHENG LONGSHENG; LI SHUO; YU JIANCHAO; LU BIN 权利人:SHENZHEN CATALYS TECH CO LTD; SHENZHEN GREENCAT PHARMACEUTICAL TECH CO LTD 摘要:Provided herein are a 2, 3-dihydrobenzo[d][1, 3]oxaphosphole derivative of formula (I) and a preparation method thereof. Compound I was constructed in utilizing tandem nucleophilic addition (or nucleophilic substitution) and intramolecular S NAr reaction. The method has the characteristics of simple operation steps, high yield, and mild reaction conditions. The technical problems of complex and harsh conditions in the synthesis of oxaphosphinine compounds in a conventional prior art were solved.
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合成参考文献
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