Enantioselective synthesis of (1S,2R)-ephenamine

被引：12
|
作者：
Kaur, Ramandeep [1 ]
Pandey, Satyendra Kumar [1 ]
机构：
[1] Thapar Univ, Sch Chem & Biochem, Patiala 147001, Punjab, India
来源：
TETRAHEDRON-ASYMMETRY | 2016年 / 27卷 / 7-8期
关键词：
ALPHA-AMINO-ACIDS; PRACTICAL CHIRAL AUXILIARY; ASYMMETRIC-SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; TRANSFER HYDROGENATION; DERIVATIVES; PSEUDOEPHEDRINE; DIHYDROXYLATION; ALKYLATION; ALCOHOLS;
D O I：
10.1016/j.tetasy.2016.02.013
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
A short and efficient enantioselective synthesis of (15,2R)-ephenamine is described employing Sharpless asymmetric dihydroxylation and regioselective nucleophilic opening of a cyclic sulfite as the key steps. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码：338 / 340
页数：3
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