NEW METHODS IN PEPTIDE-SYNTHESIS, BASED ON SUPERNUCLEOPHILES

被引：23

作者：

ECKERT, H

BREUER, W

GELLER, J

LAGERLUND, I

LISTL, M

MARQUARDING, D

STUBER, S

UGI, I

ZAHR, S

ZYCHLINSKI, HV

机构：

[1] Organisch-Chemisches Institut, Technische Universität München, Garching, Lichtenbergstr. 4

来源：

PURE AND APPLIED CHEMISTRY | 1979年 / 51卷 / 06期

关键词：

D O I：

10.1351/pac197951061219

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The fragmentation of β-halogenated alkyl groups and δ-halogenated butenvl groups from the N- and C-termini of a-amino acids and peptide derivatives by the supernucleophilic CoI-phthalocyanine-phthalocyanine anion as well as related reactions are presented as the basis of some new protecting group techniques and synthetic methods for peptides. © IUPAC

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页码：1219 / 1233

页数：15

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