A general synthesis of oligopeptides containing an oxirane ring in the place of a peptidic bond

被引：15

作者：

Mann, A

Quaranta, L

Reginato, G

Taddei, M

机构：

[1] UNIV SASSARI,DIPARTIMENTO CHIM,I-07100 SASSARI,ITALY

[2] CNRS,CTR NEUROCHIM,LAB PHARMACOCHIM MOLEC,F-67084 STRASBOURG,FRANCE

[3] UNIV FLORENCE,DIPARTIMENTO CHIM ORGAN UGO SCHIFF,I-50121 FLORENCE,ITALY

[4] CNR,CTR CHIM COMPOSTI ETEROCICLICI & LORO APPLICAZ,I-50121 FLORENCE,ITALY

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 15期

关键词：

D O I：

10.1016/0040-4039(96)00352-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Molecules structurally analogous to dipeptides, containing an oxirane ring in the place of the peptidic bond, can be prepared by oxidative conversion of beta-hydroxyselenides obtained by Mukaiyama aldol type reaction of N-protected beta-amino alpha-selenyl aldehydes derived from naturally occurring amino acids. Copyright (C) 1996 Elsevier Science Ltd

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页码：2651 / 2654

页数：4

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