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
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
引用
收藏
页码:1219 / 1233
页数:15
相关论文
共 46 条
[41]   UBER TRIPHENYL-PHOSPHINMETHYLENE ALS OLEFINBILDENDE REAGENZIEN .1. [J].
WITTIG, G ;
SCHOLLKOPF, U .
CHEMISCHE BERICHTE-RECUEIL, 1954, 87 (09) :1318-1330
[42]   TOTAL SYNTHESIS OF CEPHALOSPORIN C [J].
WOODWARD, RB ;
HEUSLER, K ;
GOSTELI, J ;
NAEGELI, P ;
OPPOLZER, W ;
RAMAGE, R ;
RANGANAT.S ;
VORBRUGG.H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (04) :852-&
[43]  
WUNSCH E, 1974, METHODEN ORGANISCHEN, V15
[44]  
ZAHR S, 1978, THESIS TU MUNCHEN
[45]  
ZYCHLINSKI HV, UNPUBLISHED
[46]  
ZYCHLINSKI HV, 1974, ANGEW CHEM, V86, P517