Highly diastereoselective synthesis of quaternary alpha-trifluoromethyl alpha-amino acids by addition of benzylzinc reagents to chiral imines of trifluoropyruvate
Yang J(杨洁) ; Min QQ(闵巧桥) ; HE YI ; Zhang XG(张新刚)
刊名Tetrahedron Lett.
2011
卷号52期号:36页码:4675-4677
ISSN号0040-4039
其他题名通过苄基锌试剂对手性三氟丙酮酸酯亚胺高立体选择性加成合成具有季碳手心的a-氨基酸
通讯作者张新刚
英文摘要An effective and facile method for highly diastereoselective synthesis of quaternary alpha-trifluoromethyl alpha-amino acids was developed in good yields with high diastereoselectivity (dr >20:1) via MgCl(2)-accelerated addition of benzylzinc reagents (Knochel type organozinc reagents) to (R)-phenylglycinol methyl ether based imines of trifluoropyruvate. (C) 2011 Elsevier Ltd. All rights reserved.
学科主题氟化学 ; 金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tetlet.2011.07.006
语种英语
WOS记录号WOS:000294145600022
公开日期2013-08-23
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/28219]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Yang J,Min QQ,HE YI,et al. Highly diastereoselective synthesis of quaternary alpha-trifluoromethyl alpha-amino acids by addition of benzylzinc reagents to chiral imines of trifluoropyruvate[J]. Tetrahedron Lett.,2011,52(36):4675-4677.
APA 杨洁,闵巧桥,HE YI,&张新刚.(2011).Highly diastereoselective synthesis of quaternary alpha-trifluoromethyl alpha-amino acids by addition of benzylzinc reagents to chiral imines of trifluoropyruvate.Tetrahedron Lett.,52(36),4675-4677.
MLA 杨洁,et al."Highly diastereoselective synthesis of quaternary alpha-trifluoromethyl alpha-amino acids by addition of benzylzinc reagents to chiral imines of trifluoropyruvate".Tetrahedron Lett. 52.36(2011):4675-4677.
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