ACTIVE ESTERS OF 9-FLUORENYLMETHYLOXYCARBONYL AMINO-ACIDS AND THEIR APPLICATION IN THE STEPWISE LENGTHENING OF A PEPTIDE-CHAIN

被引：56

作者：

BODANSZKY, A ^{[1
]}

BODANSZKY, M ^{[1
]}

CHANDRAMOULI, N ^{[1
]}

KWEI, JZ ^{[1
]}

MARTINEZ, J ^{[1
]}

TOLLE, JC ^{[1
]}

机构：

[1] CASE WESTERN RESERVE UNIV, DEPT CHEM, CLEVELAND, OH 44106 USA

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1980年 / 45卷 / 01期

关键词：

D O I：

10.1021/jo01289a016

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：72 / 76

页数：5

共 29 条

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[5] SIDE REACTIONS IN PEPTIDE-SYNTHESIS .11. POSSIBLE REMOVAL OF THE 9-FLUORENYLMETHYLOXYCARBONYL GROUP BY THE AMINO COMPONENTS DURING COUPLING [J].

BODANSZKY, M ;

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[6] ORTHO-NITROPHENYL ESTERS OF TERT-BUTYLOXYCARBONYLAMINO ACIDS AND THEIR APPLICATION IN STEPWISE SYNTHESIS OF PEPTIDE CHAINS BY A NEW TECHNIQUE [J].

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JOURNAL OF ORGANIC CHEMISTRY, 1973, 38 (20) :3565-3570

[7] OMICRON-NITROPHENYL ESTERS OF BENZYLOXYCARBONYLAMINO ACIDS AND THEIR APPLICATION IN SYNTHESIS OF PEPTIDE CHAINS BY IN-SITU TECHNIQUE [J].

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[9]

BODANSZKY M, 1962, BIOCHEM PREP, V9, P110

[10]

BODANSZKY M, BIOORG CHEM

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