Synthesis of an epimer of a 16-membered ring model for teicoplanin: Confirmation of epimerization during cycloamidation

被引：28

作者：

Pearson, AJ

Zhang, PL

Bignan, G

机构：

[1] Department of Chemistry, Case Western Reserve University, Cleveland

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1997年 / 62卷 / 13期

关键词：

D O I：

10.1021/jo970508t

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：4536 / 4538

页数：3

共 11 条

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[4] Alternative synthesis of the cycloisodityrosine subunit of deoxybouvardin, RA-VII, and related agents: Reassignment of the stereochemistry of prior intermediates
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[5] Evans D.A., 1994, GLYCOPEPTIDE ANTIBIO, Vfirst, P63
[6] STRUCTURE OF THE MAJOR GLYCOPEPTIDE OF THE TEICOPLANIN COMPLEX
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[7] A synthesis of D,L-N,N-dimethylcycloisodityrosines: A comment on the stereochemistry of previously reported intermediates related to the synthesis of RA-VII and deoxybouvardin
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (12) : 3936 - 3937
[8] SYNTHESIS OF A 16-MEMBERED CYCLIC PEPTIDE MODEL OF THE BCF RINGS OF RISTOCETIN-A USING ARENE-RUTHENIUM CHEMISTRY COUPLED WITH CYCLOAMIDATION
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[9] Cycloetherification reactions of areneruthenium complexes: Construction of a 16-membered cyclic peptide model for teicoplanin
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (12) : 3940 - 3941
[10] PEARSON AJ, 1994, J ORG CHEM, V59, P225

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