专利号:US-7138526-B1 优先权日:1999-06-15 标 题 :Solid phase synthesis of n,n-disubstituted diazacycloalkylcarboxy derivatives 发明人:HERPIN TIMOTHY F; MORTON GEORGE C; SALVINO JOSEPH M 权利人:AVENTIS PHARMA INC 摘要:A method for the solid phase synthesis of N,N-disubstituted diazacycloalkylcarboxy derivatives of general formula (I) and (II) is claimed. Examples include piperazine-2-carboxamide. The method is applicable to the synthesis or large combinatorial libraries
专利号:EP-2918579-A1 优先权日:2014-03-14 标题 :Synthesis of 2-arylmethyl-5-aryl-thiophene 权利人:LEK PHARMACEUTICALS 摘要:The present invention provides a new synthetic process for the production of 2-arylmethyl-5-aryl-thiophene, an intermediate in the synthesis of C-aryl glycosides.
专利号:US-6372945-B1 优先权日:1995-06-07 标 题 :Process for the synthesis of vinyl sulfoxides 发明人:AIKINS JAMES A; MILLER RANDAL SCOT; ZHANG TONY Y 权利人:LILLY CO ELI 摘要:The present invention is directed to a new process for the synthesis of vinyl sulfoxides, in particular diarylvinyl sulfoxides
专利号:US-5606076-A 优先权日:1995-06-07 标 题 :Process for the synthesis of benzo[b]thiophenes 发明人:AIKINS JAMES A; ZHANG TONY Y 权利人:LILLY CO ELI 摘要:The present invention is directed to a process for the synthesis of 2-arylbenzo[b]thiophenes.
专利号:US-5569772-A 优先权日:1995-06-07 标 题:Process for the synthesis of benzo[b]thiophenes 发明人:HOARD DAVID W; LUKE WAYNE D 权利人:LILLY CO ELI 摘要:The present invention is directed to a new process for the synthesis of 2-aryl benzo[b]thiophenes, and to novel intermediates therefor.
专利号:US-5606075-A 优先权日:1995-06-07 标 题:Process for the synthesis of benzo[b]thiophenes 发明人:HOARD DAVID W; LUKE WAYNE D 权利人:LILLY CO ELI 摘要:The present invention is directed to new processes for the synthesis of 2-aryl benzo[b]thiophenes.
参考标题:Allenone-Mediated Racemization/epimerization-Free Peptide Bond Formation And Its Application In Peptide Synthesis 作者:Zhengning Wang,Xuewei Wang,Penghui Wang,Junfeng Zhao |发布日期:2021.7.14 摘要:Peptide Synthesis (Spps). The Robustness Of The Allenone-Mediated Peptide Bond Formation Was Showcased Incisively By The Synthesis Of Carfilzomib, Which Involved A Rare Racemization-/epimerization-Free N To C Peptide Elongation Strategy. Furthermore, The Successful Synthesis Of The Model Difficult Peptide Acp (65-74) On A Solid Support Suggested That This Method Was Compatible With Spps. This Method Combines
合成参考文献
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