中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
improvedsynthesisofrupintrivir

文献类型:期刊论文

作者Lin Daizong1; Qian Wangke2; Hilgenfeld Rolf1; Jiang Hualiang1; Chen Kaixian1; Liu Hong1
刊名sciencechinachemistry
出版日期2012
卷号55期号:6页码:1101
关键词RHINOVIRUS PROTEASE INHIBITOR STRUCTURE-BASED DESIGN BIOLOGICAL EVALUATION ENTEROVIRUS 71 INTERMEDIATE PROTEINASE EFFICIENT AG7088 rupintrivir AG7088 synthesis
ISSN号1674-7291
DOI10.1007/s11426-011-4478-5
英文摘要An improved synthesis of rupintrivir (AG7088) was accomplished using three amino acids (l-glutamic acid, d-4-fluorophenylalanine, and l-valine) as the building blocks. The key fragment ketomethylene dipeptide isostere was constructed with the valine derivative and phenylpropionic acid derivative, followed by coupling with a lactam derivative and an isoxazole acid chloride to provide AG7088 totally in eight steps.
资助项目[National Natural Science Foundation of China] ; [National Basic Research Program of China] ; [Chinese Academy of Sciences] ; [European Commission]
语种英语
源URL[http://119.78.100.183/handle/2S10ELR8/284800]  
专题中国科学院上海药物研究所
作者单位1.中国科学院上海药物研究所
2.沈阳药科大学
推荐引用方式
GB/T 7714
Lin Daizong,Qian Wangke,Hilgenfeld Rolf,et al. improvedsynthesisofrupintrivir[J]. sciencechinachemistry,2012,55(6):1101.
APA Lin Daizong,Qian Wangke,Hilgenfeld Rolf,Jiang Hualiang,Chen Kaixian,&Liu Hong.(2012).improvedsynthesisofrupintrivir.sciencechinachemistry,55(6),1101.
MLA Lin Daizong,et al."improvedsynthesisofrupintrivir".sciencechinachemistry 55.6(2012):1101.

入库方式: OAI收割

来源:上海药物研究所

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