反-2-丁烯置于双氧水体系中,化学反应生成(R)-(-)-2-丁醇 参考文献:Hydroboration. 85. Synthesis And Hydroboration Of (-)-2-Phenylapopinene. Comparison Of Mono(2-Phenylapoisopinocampheyl)Borane With Its 2-Methyl And 2-Ethyl Analogs For The Chiral Hydroboration Of Representative Alkenes 标题:Hydroboration. 85. Synthesis And Hydroboration Of (-)-2-Phenylapopinene. Comparison Of Mono(2-Phenylapoisopinocampheyl)Borane With Its 2-Methyl And 2-Ethyl Analogs For The Chiral Hydroboration Of Representative Alkenes 摘要: Doi:10.1021/jo00291A021
专利号:WO-9006311-A1 优先权日:1988-11-29 标 题 :Synthesis of (-)-swainsonine and intermediate compounds employed in such synthesis 发明人:CHA JIN KUN; BENNETT RICHARD BERNARD III 权利人:UNIV VANDERBILT 摘要:A method of synthesizing swainsonine and its analogues employing a unique intermediate imine and a unique intermediate enamide.
专利号:US-2018111938-A1 优先权日:2015-05-05 标 题:Synthesis of Intermediates Used in the Manufacture of Anti-HIV Agents 发明人:PRADHAN BRAJA SUNDAR; AMARNATH KOMMIREDDY; VEMPALA NARESH; RAHMAN MD ATAUR 权利人:CBZ INVEST LTD 摘要:The present invention relates to a process of preparing intermediates of Formula (I). The process comprises of reacting compound of Formula (III) with compound of Formula (V) in the presence of a solvent selected from an alcohol, ether or water to form compound of Formula (I) wherein, R 1 is selected from —NH 2 , Cl, Br, NHCOR″, wherein R″ is alkyl, aryl, Schiff's base of formula Nâ•?CHR′, wherein R′ is alkyl or aryl; R 2 is selected from H, alkyl; R 3 and R 4 , each independently is H; R 5 and R 6 , each independently is H, alkyl; R 7 is H, alkyl; and R 8 is H, alkyl.
专利号:US-8653282-B2 优先权日:2007-10-18 标 题:Preparation of dihydrothieno [3,2-D] pyrimidines and intermediates used therein 发明人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G 权利人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G; BOEHRINGER INGELHEIM INT 摘要:The invention relates to improved methods of preparing dihydrothienopyrimidines of formula 1, and intermediates thereof, (I) wherein X is SO or SO 2 , preferably SO, and wherein R A , R 1 , R 2 , R 3 , R 4 and R 5 have the meanings given in the description. The methods according to this invention are more suitable for large-scale synthesis of said compounds than prior methods because the new synthetic process avoids distillation and chromatographic purification between steps and results in a higher overall yield of the desired product.
专利号:US-6255092-B1 优先权日:1993-09-24 标题:Stereospecific alcohol dehydrogenase isolated from Candida parapsilosis, amino acid and DNA sequences therefor, and method of preparation thereof 发明人:KOJIMA TOMOKO; YAMAMOTO HIROAKI; KAWADA NAOKI; MATSUYAMA AKINOBU 权利人:DAICEL CHEM 摘要:The present invention provides a novel secondary alcohol dehydrogenase useful for the synthesis of optically active alcohol and DNA encoding said enzyme. A microorganism belonging to genus Candida was found to produce a novel secondary alcohol dehydrogenase with a high stereochemical specificity. Using said enzyme, optically active alcohols were prepared, and by cloning of DNA encoding said enzyme, the base sequence of said DNA was determined. By providing a novel secondary alcohol dehydrogenase with a high stereochemical specificity and the gene encoding said enzyme, an efficient production of optically active alcohols became possible.
专利号:US-2005192265-A1 优先权日:2003-03-20 标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds 发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J 摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
专利号:US-6906056-B2 优先权日:1998-06-22 标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds 发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J 权利人:LILLY CO ELI 摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
参考标题:Purification And Characterization Of An Nadh-Dependent Alcohol Dehydrogenase FromCandida MarisFor The Synthesis Of Optically Active 1-(Pyridyl)Ethanol Derivatives 作者:Shigeru Kawano,Miho Yano,Junzo Hasegawa,Yoshihiko Yasohara |发布日期:2011.6.23 摘要:A Novel (R)-Specific Alcohol Dehydrogenase (Afpdh) Produced By Candida Maris Ifo10003 Was Purified To Homogeneity By Ammonium Sulfate Fractionation, Deae-Toyopearl, And Phenyl-Toyopearl, And Characterized. The Relative Molecular Mass Of The Native Enzyme Was Found To Be 59,900 By Gel Filtration, And That Of The Subunit Was Estimated To Be 28,900 On Sds-Polyacrylamide Gel Electrophoresis. These Results Suggest That The Enzyme Is A Homodimer. It Required Nadh As A Cofactor And Reduced Various Kinds Of Carbonyl Compounds, Including Ketones And Aldehydes. Afpdh Reduced Acetylpyridine Derivatives, β-Keto Esters, And Some Ketone Compounds With High Enantioselectivity. This Is The First Report Of An Nadh-Dependent, Highly Enantioselective (R)-Specific Alcohol Dehydrogenase Isolated From A Yeast. Afpdh Is A Very Useful Enzyme For The Preparation Of Various Kinds Of Chiral Alcohols.