ARYL AZIDES AS PHOTOLABELS - RETENTION OF IODINE DURING PHOTOCHEMICAL RING EXPANSION OF AN IODINATED TYROSINE DERIVATIVE

被引：11

作者：

HENRIKSEN, U ^{[1
]}

BUCHARDT, O ^{[1
]}

机构：

[1] UNIV COPENHAGEN,HC ORSTED INST,CTR MED BIOTECHNOL,UNIV PK 5,DK-2100 COPENHAGEN,DENMARK

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 17期

关键词：

D O I：

10.1016/S0040-4039(00)97384-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

In contrast to the photochemical behaviour of iodinated aromatic azides with iodine and azide in the same ring, iodinated N-(4-azidobenzoyl)tyrosine readily undergoes singlet photochemistry with ring expansion and trapping of nucleophiles while retaining iodine substituents in the phenol nucleus. © 1990.

引用

页码：2443 / 2444

页数：2

共 6 条

[1]

BUCHARDT O, 1989, NATO ADV SCI I C-MAT, V272, P1

[2]

IMAI N, IN PRESS BIOCONJUGAT

[3] ARYL AZIDES AS PHOTOAFFINITY LABELS - A PHOTOCHEMICAL STUDY OF SOME 4-SUBSTITUTED ARYL AZIDES [J].

NIELSEN, PE ;

BUCHARDT, O .

PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1982, 35 (03) :317-323

[4] A I-125 RADIOLABEL TRANSFER CROSSLINKING REAGENT WITH A NOVEL CLEAVABLE GROUP [J].

SCHWARTZ, MA .

ANALYTICAL BIOCHEMISTRY, 1985, 149 (01) :142-152

[5]

SUNESON E, UNPUB

[6] EXPLORATORY PHOTOCHEMISTRY OF IODINATED AROMATIC AZIDES [J].

WATT, DS ;

KAWADA, K ;

LEYVA, E ;

PLATZ, MS .

TETRAHEDRON LETTERS, 1989, 30 (08) :899-902

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