PEPTIDES .36. SYNTHESIS OF THE 27-37 FRAGMENT OF A LYSOZYME ANALOG

被引：9

作者：

GALPIN, IJ

KENNER, GW

OHLSEN, SR

RAMAGE, R

SHEPPARD, RC

TYSON, RG

机构：

[1] The Robert Robinson Laboratories, University of Liverpool, Liverpool, England

来源：

TETRAHEDRON | 1979年 / 35卷 / 23期

关键词：

D O I：

10.1016/0040-4020(79)80137-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Two syntheses of the fully protected 27-37 fragment have been carried out. The results indicate that coupling of the 27-32 and 33-37 fragments is superior to the alternative 27-29 plus 30-37 approach. © 1979.

引用

页码：2785 / 2790

页数：6

共 11 条

[1] AMINO-ACIDS AND PEPTIDES .37. TRIFLUOROACETYLATION DURING COUPLING OF TERT-BUTOXYCARBONYLAMINO-ACIDS WITH PEPTIDE ESTERS IN PRESENCE OF TRIFLUOROACETATE ANION
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[7] UBER DIE GESCHWINDIGKEIT DER AMINOLYSE VON VERSCHIEDENEN NEUEN, AKTIVIERTEN, N-GESCHUTZTEN ALPHA-AMINOSAURE-PHENYLESTERN, INSBESONDERE 2,4,5-TRICHLORPHENYLESTERN
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1973, (23): : 2890 - 2894
[9] PEPTIDE SYNTHESIS VIA 2-(PARA-DIPHENYL)-ISOPROPYLOXYCARBONYL (DPOC)-AMINO PROTECTING GROUPS
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[J]. HELVETICA CHIMICA ACTA, 1968, 51 (04) : 622 - &
[10] SYNTHESIS OF 2-(PARA-BIPHENYLYL)ISOPROPYLOXYCARBONYLAMINO ACIDS AND DECOMPOSITION OF ARALKYL PHENYL CARBONATES
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