Highly diastereoselective radical cyclisations of chiral sulfinimines

被引：23

作者：

Rochette, Elise M. ^{[1
]}

Lewis, William ^{[1
]}

Dossetter, Al G. ^{[2
]}

Stockman, Robert A. ^{[1
]}

机构：

[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England

[2] AstraZeneca, Macclesfield SK10 4TG, Cheshire, England

来源：

CHEMICAL COMMUNICATIONS | 2013年 / 49卷 / 82期

基金：

英国工程与自然科学研究理事会;

关键词：

ASYMMETRIC-SYNTHESIS; ALDIMINES; EFFICIENT; ALCOHOLS; IMINES;

D O I：

10.1039/c3cc45452e

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Chiral amines are formed by the highly diastereoselective intramolecular addition of alkyl and aryl radicals onto chiral mesityl sulfinimines.

引用

页码：9395 / 9397

页数：3

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