3162-96-7 = 97-30-3 反应条件:1.1 Catalysts: Methanesulfonic Acid,1,1,1-Trifluoro-,Erbium(3+) Salt (3:1) Solvents: Acetonitrile; 2.5 H,Rt 标题:Mild And Efficient Method For The Cleavage Of Benzylidene Acetals By Using Erbium(Iii) Triflate 作者:Procopio,Antonio; Dalpozzo,Renato; De Nino,Antonio; Maiuolo,Loredana; Nardi,Monica; Et Al 参考文献:Organic & Biomolecular Chemistry 日期:2005 卷标:3(22) 页码:4129-4133]
13035-25-1 = 97-30-3 反应条件:1.1 Reagents: Dimethylbarbituric Acid Catalysts: Tetrakis(Triphenylphosphine)Palladium Solvents: Methanol; 1 H,Rt 标题:Remarkable Solvent Effect On Pd(0)-Catalyzed Deprotection Of Allyl Ethers Using Barbituric Acid Derivatives: Application To Selective And Successive Removal Of Allyl,Methallyl,And Prenyl Ethers 作者:Tsukamoto,Hirokazu; Suzuki,Takamichi; Kondo,Yoshinori 参考文献:Synlett 日期:2007 卷标:(20) 页码:3131-3136]
57701-27-6 = 97-30-3 反应条件:1.1 Reagents: 1-Phenyl-1,2-Ethanediol,Dibenzyl,P-Toluenesulfonic Acid Solvents: Dichloromethane,Water 标题:Transacetalation: A Convenient,Nonaqueous Method For Effecting The Deprotection Of Isopropylidene And Benzylidene Derivatives Of Sugars 作者:Andrews,Mark A.; Gould,George L. 参考文献:Carbohydrate Research 日期:1992 卷标:229(1) 页码:141-7]
专利号:US-4910310-A 优先权日:1988-10-03 标 题:Synthesis of N-substituted 1,5-dideoxy-1,5-imino-L-fucitol derivatives 发明人:CAMPBELL ARTHUR L; BEHLING JAMES R; BABIAK KEVIN A; NG JOHN S; MUELLER RICHARD A; FLEET GEORGE W J 权利人:SEARLE & CO 摘要:Novel intermediates and method for the chemical synthesis of N-substituted 1,5-dideoxy-1,5-imino-L-fucitol derivatives are provided. A preferred intermediate is 1,5-dideoxy-1,5-imino-3, 4-O-isopropylidene-L-fucitol which is used to prepare the HIV inhibitor 1,5-dideoxy-1,5-imino-[N-ω-methyl caproate]-L-fucitol. These compounds are prepared in a short synthesis from the known compound 2,3-O-isopropylidene-D-lyxono-1,4-lactone or in a multi-step synthesis from D-galactose.
专利号:US-7943594-B2 优先权日:2002-07-10 标 题 :Solid-phase and solution-phase synthesis of glycosylphosphatidylinositol glycans 发明人:SEEBERGER PETER H; HEWITT MICHAEL C; SNYDER DANIEL A 权利人:MASSACHUSETTS INST TECHNOLOGY 摘要:One aspect of the present invention relates to solution-phase approaches to GPI synthesis. Another aspect of the present invention relates to key building blocks, and syntheses thereof, useful for GPI assembly. Yet another aspect of the invention relates to an automated method for the synthesis of GPIs and fragments thereof.
专利号:US-4384998-A 优先权日:1981-03-30 标题:Synthesis of thienamycin from D-glucose 发明人:DURETTE PHILIPPE L 权利人:MERCK & CO INC 摘要:Disclosed is a chiral, total synthesis of thienamycin from D-glucose which proceeds via intermediates I, II and III to known aldehyde IV which is known to be useful in the total synthesis of thienamycin (V): ##STR1## wherein: R is lower alkyl having 1-6 carbon atoms or bi-valent alkyl having 2-6 carbon atoms which joins the two sulfur atoms; R 1 is lower alkyl or aralkyl, such as benzyl and the like; and R 2 is hydrogen or a removable protecting group, such as triorganosilyl wherein the organo groups are independently selected from lower alkyl, phenyl and phenylloweralkyl.
专利号:US-4448976-A 优先权日:1981-03-30 标题 :Chiral synthesis of thienamycin from D-gluocose 发明人:DURETTE PHILIPPE L 权利人:MERCK & CO INC 摘要:Disclosed is a chiral, total synthesis of thienamycin from D-glucose which proceeds via intermediates I, II and III to known aldehyde IV which is known to be useful in the total synthesis of thienamycin (V): ##STR1## wherein: R is lower alkyl having 1-6 carbon atoms or bi-valent alkyl having 2-6 carbon atoms which joins the two sulfur atoms; R 1 is lower alkyl or aralkyl, such as benzyl and the like; and R 2 is hydrogen or a removable protecting group, such as triorganosilyl wherein the organo groups are independently selected from lower alkyl, phenyl and phenylloweralkyl.
专利号:US-4544502-A 优先权日:1981-03-30 标 题 :Chiral synthesis of thienamycin from D-glucose 发明人:DURETTE PHILIPPE L 权利人:MERCK & CO INC 摘要:Disclosed is a chiral, total synthesis of thienamycin from D-glucose which proceeds via intermediates I, II and III to known aldehyde IV which is known to be useful in the total synthesis of thienamycin (V): ##STR1## wherein: R is lower alkyl having 1-6 carbon atoms or bi-valent alkyl having 2-6 carbon atoms which joins the two sulfur atoms; R 1 is lower alkyl or aralkyl, such as benzyl and the like; and R 2 is hydrogen or a removable protecting group, such as triorganosilyl wherein the organo groups are independently selected from lower alkyl, phenyl and phenylloweralkyl.
专利号:US-4256646-A 优先权日:1978-06-29 标题:Synthesis of optically pure thromboxanes 发明人:HERNANDEZ OSCAR; BEND JOHN R; ELING THOMAS E; MCKINNEY JAMES D 权利人:US HEALTH EDUCATION & WELFARE 摘要:In an elegant stepwise process for the production of intermediates of thromboxanes such as TXB 2 from a chiral glucose starting material such as α-methylglucoside, those steps comprising: ##STR1## A key modification introduced in this synthetic sequence is the use of 4-dimethylaminopyridine for the selective alkylation of primary alcohols in the presence of unprotected secondary alcohols and for the controlled acylation of methylglucoside. The former application has large potential use in the synthesis of nucleosides, polynucleotides, and carbohydrate derivatives.