PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE-SYNTHESIS - USE OF A NEW DERIVATIVE, N-IN-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHAN

被引：16

作者：

KISO, Y

INAI, M

KITAGAWA, K

AKITA, T

机构：

来源：

CHEMISTRY LETTERS | 1983年 / 05期

关键词：

D O I：

10.1246/cl.1983.739

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：739 / 742

页数：4

共 19 条

[1]

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[2]

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[3]

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[4]

Geiger R, 1981, PEPTIDES, V3, P82

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[6]

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[7] AN ACTIVE ESTER-TYPE MIXED ANHYDRIDE METHOD FOR PEPTIDE-SYNTHESIS - USE OF THE NEW REAGENT, NORBORN-5-ENE-2,3-DICARBOXIMIDO DIPHENYL PHOSPHATE (NDPP) [J].

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[8] EFFICIENT REMOVAL OF N-BENZYLOXYCARBONYL GROUP BY A PUSH-PULL MECHANISM USING THIOANISOLE-TRIFLUOROACETIC ACID, EXEMPLIFIED BY A SYNTHESIS OF MET-ENKEPHALIN [J].

KISO, Y ;

UKAWA, K ;

AKITA, T .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1980, (03) :101-102

[9] CROWN ETHERS AS CATALYSTS OF FLUORIDE-ANION-MEDIATED REACTIONS IN PEPTIDE-SYNTHESIS .1. PROTECTION OF TRYPTOPHAN BY BENZYLOXYCARBONYL AND 2,4-DICHLOROBENZYLOXYCARBONYL GROUPS [J].

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CHOREV, M .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1977, (06) :627-631

[10] STUDIES ON THE NIN-FORMYL GROUP AS POSSIBLE PROTECTING GROUP AGAINST TRYPTOPHAN INDOLE SIDE-CHAIN TERT-BUTYLATION [J].

LOW, M ;

KISFALUDY, L .

HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1979, 360 (01) :13-18

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