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SYNTHETIC STUDIES ON THE AZINOTHRICIN FAMILY OF ANTIBIOTICS .3. ENANTIOSELECTIVE SYNTHESIS OF A HEXAPEPTIDE PRECURSOR FOR ANTITUMOR ANTIBIOTIC A83586C

被引：28
作者：
HALE, KJ
DELISSER, VM
YEH, LK
PEAK, SA
MANAVIAZAR, S
BHATIA, GS
机构：
[1] The Christopher Ingold Laboratories, Department of Chemistry, University College London, London, WC1H 0AJ England
来源：
TETRAHEDRON LETTERS | 1994年 / 35卷 / 41期
关键词：
D O I：
10.1016/S0040-4039(00)78375-4
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A ''3+2+1'' fragment condensation strategy to a precursor of the hexapeptide f
引用
收藏
页码：7685 / 7688
页数：4
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