Chemoenzymatic approaches to the dynamic kinetic asymmetric synthesis of aromatic amino acids

被引:24
作者
Chaplin, JA
Levin, MD
Morgan, B
Farid, N
Li, J
Zhu, ZL
McQuaid, J
Nicholson, LW
Rand, CA
Burk, MJ
机构
[1] Diversa Corp, San Diego, CA 92121 USA
[2] Dow Chem Co USA, Midland, MI 48667 USA
关键词
D O I
10.1016/j.tetasy.2004.07.060
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Enzymatic approaches for the production of amino acids by nitrilases Lire described. Dynamic kinetic asymmetric synthesis conditions were established for the aromatic aminonitriles, phenylglycinonitrile and 4-fluorophenylglycinonitrile, at high pH to produce the corresponding amino acid products in high enantiomeric excess. N-Acylation of aromatic aminonitriles led to spontaneous racemization at pH 8, allowing preferential enzymatic hydrolysis of the (R)-enantiomer to afford the product N-acyl-amino acids in Lip to 99% enantiomeric excess (ee). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2793 / 2796
页数:4
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