中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis of optically active beta-alkyl-alpha-methylene-gamma-butyrolactones from enantioselective biotransformation of nitriles, an unusual inversion of enantioselectivity

文献类型:期刊论文

作者Zhao, SM; Wang, MX
刊名CHINESE JOURNAL OF CHEMISTRY
出版日期2002-11-01
卷号20期号:11页码:1291-1299
关键词Biotransformation Nitrile Hydratase Amidase Optically Active Beta-alkyl-alpha-methylene-gamma-butyrolactone Inversion Of Enantioselectivity
ISSN号1001-604X
英文摘要A new approach to optically active beta-alltyl-alpha-methylene-gamma-bu-tyrolactone derivatives was reported from the Rhodococcus sp. AJ270-catalyzed hydrolysis of appropriate nitriles. The inversion of enantioselectivity of the amidase has been observed when a methyl protection was introduced into the hydroxy group of the parent substrate.
语种英语
WOS记录号WOS:000179210800024
出版者SCIENCE CHINA PRESS
源URL[http://ir.iccas.ac.cn/handle/121111/78327]  
专题中国科学院化学研究所
通讯作者Wang, MX
作者单位Chinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
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Zhao, SM,Wang, MX. Synthesis of optically active beta-alkyl-alpha-methylene-gamma-butyrolactones from enantioselective biotransformation of nitriles, an unusual inversion of enantioselectivity[J]. CHINESE JOURNAL OF CHEMISTRY,2002,20(11):1291-1299.
APA Zhao, SM,&Wang, MX.(2002).Synthesis of optically active beta-alkyl-alpha-methylene-gamma-butyrolactones from enantioselective biotransformation of nitriles, an unusual inversion of enantioselectivity.CHINESE JOURNAL OF CHEMISTRY,20(11),1291-1299.
MLA Zhao, SM,et al."Synthesis of optically active beta-alkyl-alpha-methylene-gamma-butyrolactones from enantioselective biotransformation of nitriles, an unusual inversion of enantioselectivity".CHINESE JOURNAL OF CHEMISTRY 20.11(2002):1291-1299.

入库方式: OAI收割

来源:化学研究所

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