ICCAS OpenIR
Highly efficient and enantioselective synthesis of L-arylglycines and D-arylglycine amides from biotransformations of nitriles
Wang, MX; Lin, SJ
2001-09-24
Source PublicationTETRAHEDRON LETTERS
ISSN0040-4039
Volume42Issue:39Pages:6925-6927
AbstractUnder very mild conditions, the Rhodococcus sp. AJ270-catalysed biotransformation of arylglycine nitriles 1, prepared easily from the reaction of substituted benzaldehydes, ammonium chloride and potassium cyanide, proceeded efficiently to produce optically active D-arylglycine amides 2 and L-arylglycines 3 in excellent yields with enantiomeric excesses higher than 99%. (C) 2001 Elsevier Science Ltd. All rights reserved.
Indexed ByCCR ; SCI
Language英语
WOS IDWOS:000171083500035
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/76596
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,Lin, SJ. Highly efficient and enantioselective synthesis of L-arylglycines and D-arylglycine amides from biotransformations of nitriles[J]. TETRAHEDRON LETTERS,2001,42(39):6925-6927.
APA Wang, MX,&Lin, SJ.(2001).Highly efficient and enantioselective synthesis of L-arylglycines and D-arylglycine amides from biotransformations of nitriles.TETRAHEDRON LETTERS,42(39),6925-6927.
MLA Wang, MX,et al."Highly efficient and enantioselective synthesis of L-arylglycines and D-arylglycine amides from biotransformations of nitriles".TETRAHEDRON LETTERS 42.39(2001):6925-6927.
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