专利号:US-5012000-A 优先权日:1989-10-30 标 题 :Total synthesis of chiral 2-amino-1,3-diols 发明人:ILLIG CARL R; WEIS ALEXANDER L 权利人:EASTMAN KODAK CO 摘要:A method for the preparation of chiral 2-amino-1,3-diols is disclosed. The method involves four steps including performance of an aldol condensation with a chiral oxazolidinone on an aldehyde, treating the aldol condensation product with an alkali metal azide, treating the product with a borohydride reagent and reducing the azide to an amine.
专利号:WO-0053313-A2 优先权日:1999-03-09 标 题:Lanthanide catalysts for synthesis of compounds and combinatorial libraries
专利号:KR-20090097208-A 优先权日:2006-12-31 标 题:Process for the synthesis of derivatives of 3-amino-tetrahydrofuran-3-carboxylic acid and use thereof as medicaments
专利号:CN-108840854-B 优先权日:2018-09-18 标 题 :A kind of method for one-pot synthesis of 5-chlorothiophene-2-carboxylic acid
专利号:WO-2008080891-A2 优先权日:2006-12-31 标 题:Process for the synthesis of derivatives of 3-amino-tetrahydrofuran-3-carboxylic acid and use thereof as medicaments
专利号:US-4681891-A 优先权日:1984-11-27 标 题 :Dihydro-2,6-dimethyl pyridines, formulations and method of use for treating angina pectoris, high blood pressure or disturbances of cerebral or peripheral blood flow 发明人:SCHOENAFINGER KARL; BOHN HELMUT; MARTORANA PIERO; NITZ ROLF-EBERHARD 权利人:CASSELLA FARBWERKE MAINKUR AG 摘要:1,4-dihydropyridines of the formula I (I) wherein R1 denotes optionally substituted phenyl, pyridyl or thienyl, R2 denotes optionally substituted oxadiazolyl, thiadiazolyl or thiazolyl and R3 denotes hydrogen or -COOH, their preparation by a modified Hantzsch synthesis and their use as a calcium-agonist in pharmacy.
参考标题:Diversity Oriented Clicking (Doc): Divergent Synthesis Of Sufexable Pharmacophores From 2‐substituted‐alkynyl‐1‐sulfonyl Fluoride (Sasf) Hubs 作者:Christopher J. Smedley,Gencheng Li,Andrew S. Barrow,Timothy L. Gialelis,Marie‐claire Giel,Alessandra Ottonello,Yunfei Cheng,Seiya Kitamura,Dennis W. Wolan,K. Barry Sharpless,John E. Moses |发布日期:2020.7.20 摘要:Diversity Oriented Clicking (Doc) Is A Unified Click‐approach For The Modular Synthesis Of Lead‐like Structures Through Application Of The Wide Family Of Click Transformations. Doc Evolved From The Concept Of Achieving "Diversity With Ease" , By Combining Classic C−c π‐bond Click Chemistry With Recent Developments In Connective Sufex‐technologies. We Showcase 2‐substituted‐alkynyl‐1‐sulfonyl Fluorides
合成参考文献
摘要:Li, Y.; Xie, W.; Jiang, X., Science of Synthesis Knowledge Updates, (2016) 2, 82. 摘要:Lubell, W. D.; St-Cyr, D. J.; Dufour-Gallant, J.; Hopewell, R.; Boutard, N.; Kassem, T.; Dörr, A.; Zelli, R., Science of Synthesis Knowledge Updates, (2013) 1, 307. 摘要:Schatz, J.; Seler, M., Science of Synthesis Knowledge Updates, (2011) 2, 404. 摘要:Pitaval, A.; Echavarren, A. M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 542. 摘要:Denmark, S.; Chang, W.-T. T., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 419.