Stereoselective synthesis of ferrocenylamino acids

被引：13

作者：

Adamczyk, M ^{[1
]}

Reddy, RE ^{[1
]}

Rege, SD ^{[1
]}

机构：

[1] Abbott Labs, Div Diagnost, Div Organ Chem Res 9NM AP20, Abbott Pk, IL 60064 USA

来源：

SYNTHETIC COMMUNICATIONS | 2000年 / 30卷 / 08期

关键词：

D O I：

10.1080/00397910008087166

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Enantiopure ferrocenyl-beta, and bis-beta-amino acids [(R)-(+)-1 and (R,R)-(+)-2] were prepared from (S)-(+)-sulfinimine (3) and (S,S)(+)-bis-sulfinimine (4) respectively. The desired sulfinimines [(S)-(+)-3 and (S,S)-(+)-4] Mere prepared from (S)-Andersen reagent (5) and ferrocenecarboxaldehyde (6) and 1,1'-ferrocenedicarboxaldehyde (7).

引用

页码：1389 / 1400

页数：12

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