ICCAS OpenIR
Enantioselective synthesis of chiral cyclopropane compounds through microbial transformations of trans-2-arylcyclopropanecarbonitriles
Wang, MX; Feng, GQ
2000-08-12
Source PublicationTETRAHEDRON LETTERS
ISSN0040-4039
Volume41Issue:33Pages:6501-6505
AbstractEnantioselective biotransformations of racemic trans-2-arylcyclopropanecarbonitriles catalyzed by Rhodococcus sp. AJ270 cells proceeded efficiently to give good to excellent optical yields of (-)-(1R,2R)-2-arylcyclopropanecarboxamides and (+)-(1S,21S)-2-arylcyclopropanecarboxylic acids, which were converted into optically active cyclopropylmethylamine and cyclopropylamine derivatives upon reduction and the Curtius rearrangement. (C) 2000 Elsevier Science Ltd. All rights reserved.
Indexed ByIC ; CCR ; SCI
Language英语
WOS IDWOS:000088985600050
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Cited Times:47[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/76318
Collection中国科学院化学研究所
Corresponding AuthorWang, MX
AffiliationChinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Wang, MX,Feng, GQ. Enantioselective synthesis of chiral cyclopropane compounds through microbial transformations of trans-2-arylcyclopropanecarbonitriles[J]. TETRAHEDRON LETTERS,2000,41(33):6501-6505.
APA Wang, MX,&Feng, GQ.(2000).Enantioselective synthesis of chiral cyclopropane compounds through microbial transformations of trans-2-arylcyclopropanecarbonitriles.TETRAHEDRON LETTERS,41(33),6501-6505.
MLA Wang, MX,et al."Enantioselective synthesis of chiral cyclopropane compounds through microbial transformations of trans-2-arylcyclopropanecarbonitriles".TETRAHEDRON LETTERS 41.33(2000):6501-6505.
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