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

页码：338 / 340

页数：3

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