中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Biotransformations of Three-Membered (Hetero) Cyclic Nitrites and Their Applications in Organic Synthesis

文献类型:期刊论文

作者Wang Dexian1; Wang Meixiang1,2
刊名PROGRESS IN CHEMISTRY
出版日期2010-07-01
卷号22期号:7页码:1397-1402
关键词Rhodococcus Erythropolis Aj270 Biocatalysis And Biotransformation Enantioselectivity Nitrites Amides
ISSN号1005-281X
英文摘要Enantioselective biotransformation of nitriles using nitrile hydrolyzing microbial whole cell catalysts is a powerful method for the synthesis of highly enantiopure carboxylic acids and amide derivatives. In this article, progress of Rhodococcus erythropolis AJ270-catalyzed enantioselective biotransformations of nitriles including various cyclopropane-, oxirane-, and aziridine-containing carbonitriles is summarized. On the basis of the outcomes of the biotransformation study, it is proposed that a readily reachable reactive site be embedded within the spacious pocket of the nitrile hydratase while the amidase might comprise a relatively deep-buried and size-limited active site. Applications of enantioselective biotransformations of nitriles in the synthesis of natural and bioactive products are also discussed.
语种英语
WOS记录号WOS:000280274000012
出版者CHINESE ACAD SCIENCES
源URL[http://ir.iccas.ac.cn/handle/121111/70191]  
专题中国科学院化学研究所
通讯作者Wang Meixiang
作者单位1.Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
2.Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
推荐引用方式
GB/T 7714
Wang Dexian,Wang Meixiang. Biotransformations of Three-Membered (Hetero) Cyclic Nitrites and Their Applications in Organic Synthesis[J]. PROGRESS IN CHEMISTRY,2010,22(7):1397-1402.
APA Wang Dexian,&Wang Meixiang.(2010).Biotransformations of Three-Membered (Hetero) Cyclic Nitrites and Their Applications in Organic Synthesis.PROGRESS IN CHEMISTRY,22(7),1397-1402.
MLA Wang Dexian,et al."Biotransformations of Three-Membered (Hetero) Cyclic Nitrites and Their Applications in Organic Synthesis".PROGRESS IN CHEMISTRY 22.7(2010):1397-1402.

入库方式: OAI收割

来源:化学研究所

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