SOLID-PHASE PHOSPHORYLATION OF A PEPTIDE BY THE H-PHOSPHONATE METHOD

被引:22
作者
LARSSON, E [1 ]
LUNING, B [1 ]
机构
[1] UNIV STOCKHOLM,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN
关键词
D O I
10.1016/S0040-4039(00)77019-5
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The partially protected peptide SerValSerGluAla was selectively phosphorylated at Ser3 by benzyl H-phosphonate activated by pivaloyl chloride in pyridine, followed by in situ oxidation with iodine.
引用
收藏
页码:2737 / 2738
页数:2
相关论文
共 6 条
[1]   NUCLEOSIDE H-PHOSPHONATES - VALUABLE INTERMEDIATES IN THE SYNTHESIS OF DEOXYOLIGONUCLEOTIDES [J].
FROEHLER, BC ;
MATTEUCCI, MD .
TETRAHEDRON LETTERS, 1986, 27 (04) :469-472
[2]  
GAREGG PJ, 1985, CHEM SCRIPTA, V25, P280
[3]  
GAREGG PJ, 1986, CHEM SCRIPTA, V26, P58
[4]  
HAMMOND PR, 1962, J CHEM SOC, P2521
[5]  
Kemp BE, 1990, PEPTIDES PROTEIN PHO
[6]   ALTERNATIVE STRATEGIES FOR THE FMOC SOLID-PHASE SYNTHESIS OF O-4-PHOSPHO-L-TYROSINE-CONTAINING PEPTIDES [J].
KITAS, EA ;
KNORR, R ;
TRZECIAK, A ;
BANNWARTH, W .
HELVETICA CHIMICA ACTA, 1991, 74 (06) :1314-1328