75-77-4 + 288-47-1 = 79265-30-8 [标题:Reaction Conditions 标题:Product Class 17: Thiazoles 作者:Kikelj,D.; Urleb,U. 参考文献:Science Of Synthesis 日期:2002 卷标:11 页码:627-833]
75-77-4 + 3034-53-5 = 79265-30-8 反应条件:1.1 Catalysts: Butyllithium 标题:Reactions Of Trimethylsilylthiazoles With Ketens: A New Route To Regioselective Functionalization Of The Thiazole Ring 作者:Medici,Alessandro; Pedrini,Paola; Dondoni,Alessandro 参考文献:Journal Of The Chemical Society 日期:1981 卷标:(13) 页码:655-6]
75-77-4 + 3034-53-5 = 79265-30-8 反应条件:1.1 Reagents: Butyllithium Solvents: Diethyl Ether; -78 °C 标题:Synthesis Of 5-Arylthiazoles. Comparative Study Between Suzuki Cross-Coupling Reaction And Direct Arylation 作者:Primas,Nicolas; Bouillon,Alexandre; Lancelot,Jean-Charles; El-Kashef,Hussein; Rault,Sylvain 参考文献:Tetrahedron 日期:2009 卷标:65(29-30) 页码:5739-5746]
75-77-4 + 3034-53-5 = 79265-30-8 反应条件:1.1 Reagents: Butyllithium Solvents: Diethyl Ether1.2 - 标题:Synthesis Of (Trimethylsilyl)Thiazoles And Reactions With Carbonyl Compounds. Selectivity Aspects And Synthetic Utility 作者:Dondoni,Alessandro; Fantin,Giancarlo; Fogagnolo,Marco; Medici,Alessandro; Pedrini,Paola 参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(8) 页码:1748-61]
75-77-4 + 3034-53-5 = 79265-30-8 反应条件:1.1 Reagents: Butyllithium Solvents: Diethyl Ether; 30 Min,-78 °C; 30 Min,-78 °C1.2 Solvents: Diethyl Ether; -78 °C; 1 H,-78 °C; -78 °C -> Rt1.3 Reagents: Sodium Bicarbonate Solvents: Water; Rt 标题:Design And Synthesis Of A Library Of Lead-Like 2,4-Bisheterocyclic Substituted Thiophenes As Selective Dyrk/clk Inhibitors 作者:Schmitt,Christian; Kail,Dagmar; Mariano,Marica; Empting,Martin; Weber,Nadja; Et Al 参考文献:Plos One 日期:2014 卷标:9(3)]
75-77-4 + 3034-53-5 = 79265-30-8 反应条件:1.1 Catalysts: Butyllithium 标题:2-(Trimethylsilyl)Thiazole 作者:Dondoni,Alessandro; Merino,Pedro 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001
2-溴噻唑置于正丁基锂,三甲基氯硅烷体系中,用 正己烷 作为反应溶剂,化学反应生成 2-(三甲基硅基)噻唑 参考文献:N-Phosphinyl Di-And Tripeptides As Renin Inhibitors 标题:N-Phosphinyl Di-And Tripeptides As Renin Inhibitors 摘要:这项发明是新的肾素抑制剂二肽和三肽衍生物,化学式如下:
专利信息
专利号:US-7259263-B2 优先权日:2005-06-29 标题:Method of synthesis of azole-containing amino acids 发明人:HLASTA DENNIS J; ZIFICSAK CRAIG A 权利人:JANSSEN PHARMACEUTICA NV 摘要:The invention relates to methods of synthesizing 2-substituted azole compunds of formula (I): n nThe invention is also relates to compounds of formula (I) and to intermediate compounds in the synthesis method.
专利号:EP-1904465-B1 优先权日:2005-06-29 标 题 :Method of synthesis of imidazole-amino acid derivatives and related compounds 发明人:HLASTA DENNIS J; ZIFICSAK CRAIG A 权利人:JANSSEN PHARMACEUTICA NV 摘要:The invention relates to methods of synthesizing 2-substituted azole compunds of formula (I). The invention is also relates to compounds of formula (I) and to intermediate compounds in the synthesis method.
专利号:US-6683191-B2 优先权日:2000-06-05 标 题:Method for synthesis of substituted azole libraries 发明人:DENG YIJUN; HLASTA DENNIS 权利人:ORTHO MCNEIL PHARM INC 摘要:The invention relates to methods of synthesizing libraries of diverse and complex 2-substituted azole compounds of the general formula (I) or (II)wherein X, R<2 >and the ring componentsare as described herein, novel intermediates useful for synthesizing such substituted azole compounds and methods for identifying and isolating the compounds.
专利号:US-6951948-B2 优先权日:2000-06-05 标 题 :Method for synthesis of substituted azole libraries 发明人:DENG YIJUN; HLASTA DENNIS 权利人:ORTHO MCNEIL PHARM INC 摘要:The invention relates to methods of synthesizing libraries of diverse and complex 2-substituted azole compounds of the general formula (I) or (II) n n n wherein X, R 2 and the ring components n n nare as described herein, novel intermediates useful for synthesizing such substituted azole compounds and methods for identifying and isolating the compounds.
专利号:US-6020495-A 优先权日:1997-12-08 标题 :Stereoselective method for synthesizing dolaphenine 发明人:SUN XIAOYONG; SACHDEVA YESH P; WILSON DONNA KAYE; GABRIEL RICHARD L; RAM SIYA 权利人:PHARM ECO LAB INC 摘要:The present invention relates to a method for the stereospecific synthesis of an enantiomer of a chiral amine, wherein the chiral amine has the formula R 1 CH(NH 2 )R 2 . R 1 and R 2 are each independently selected from the group consisting of alkyl, aryl and heterocyclic and radicals. This method is particularly useful for stereospecifically synthesizing S-dolaphenine. The method involves contacting a chiral enantiomer of norephedrine with borane, within an aprotic solvent to form a complex for stereospecifically reducing oximes. The complex is then contacted with an oxime, thereby stereospecifically reducing said oxime to form an enantiomer of a chiral amine.
专利号:US-2007004728-A1 优先权日:2005-06-29 标题:Method of synthesis of azole-containing amino acids
摘要:Koutentis, P. A.; Ioannidou, H. A., Science of Synthesis Knowledge Updates, (2010) 1, 377. 摘要:Koutentis, P. A.; Ioannidou, H. A., Science of Synthesis Knowledge Updates, (2010) 1, 340. 摘要:Koutentis, P. A.; Ioannidou, H. A., Science of Synthesis Knowledge Updates, (2010) 1, 354. 参考文献:10.1021/ol049549j 摘要:Alcaide B, Almendros P, Redondo MC. Novel N1-C4 beta-lactam bond breakage. Synthesis of enantiopure alpha-alkoxy-gamma-keto acid derivatives. Org Lett. 2004 May 27;6(11):1765–7. doi: 10.1021/ol049549j.