[多烯大环内酯类抗生素的合成研究。1. 由碳水化合物前体合成两性霉素B的C1-C6和C7-C12片段]
[Synthetic studies of polyene macrolide antibiotics. 1. Synthesis of C1-C6- and C7-C12 fragments of amphotericin B from carbohydrate precursors].
作者信息
Sviridov A F, Romanovich A Iu, Chizhov O S
出版信息
Bioorg Khim. 1987 Dec;13(12):1665-71.
PMID:3450281
Abstract
Strategy of synthesis of polyene macrolide antibiotic amphotericin B using carbohydrates as starting material is discussed. The C1-C6 and C7-C12 fragments of amphotericin B are synthesized.
摘要
讨论了以碳水化合物为起始原料合成多烯大环内酯类抗生素两性霉素B的策略。合成了两性霉素B的C1-C6和C7-C12片段。
Zotero 插件