中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantioselective biotransformations of 2-aryl-4-pentenenitriles, a novel chemoenzymatic approach to (R)-(-)-baclofen

文献类型:期刊论文

作者Wang, MX; Zhao, SM
刊名TETRAHEDRON LETTERS
出版日期2002-09-09
卷号43期号:37页码:6617-6620
关键词Biotransformations Nitrile Hydratase Amidase Chemoenzymatic Synthesis (r)-(-)-baclofen
ISSN号0040-4039
英文摘要Catalyzed by Rhodococcus sp. AJ270 microbial cells under mild conditions, a range of racemic 2-aryl-4-pentenenitriles 1 underwent effective hydrolysis to afford excellent yields of enantiomerically pure (R)-(-)-2-aryl-4-pentenamides 2 and (S)-(+)-2-aryl-4-pentenoic acids 3 in most cases. The application of this biotransformation has been shown by a two-step synthesis of (R)-(-)-baclcfen. (C) 2002 Elsevier Science Ltd. All rights reserved.
语种英语
WOS记录号WOS:000177659700031
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://ir.iccas.ac.cn/handle/121111/78995]  
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
推荐引用方式
GB/T 7714
Wang, MX,Zhao, SM. Highly enantioselective biotransformations of 2-aryl-4-pentenenitriles, a novel chemoenzymatic approach to (R)-(-)-baclofen[J]. TETRAHEDRON LETTERS,2002,43(37):6617-6620.
APA Wang, MX,&Zhao, SM.(2002).Highly enantioselective biotransformations of 2-aryl-4-pentenenitriles, a novel chemoenzymatic approach to (R)-(-)-baclofen.TETRAHEDRON LETTERS,43(37),6617-6620.
MLA Wang, MX,et al."Highly enantioselective biotransformations of 2-aryl-4-pentenenitriles, a novel chemoenzymatic approach to (R)-(-)-baclofen".TETRAHEDRON LETTERS 43.37(2002):6617-6620.

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来源:化学研究所

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