Total synthesis of marine-derived azole resistant antifungal agent (-)-melearoride A and antibiotic (-)-PF1163B

IF 2 Q2 CHEMISTRY, ORGANIC SynOpen Pub Date : 2022-09-14 DOI:10.1055/a-1942-6969
Srihari Pabbaraja, Bharath Yasam
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引用次数: 1

Abstract

A flexible stereoselective and convergent cum divergent approach to the synthesis of two 13-membered macrolides through a common skeleton present in their structure is described in two different routes, with good overall yield. The key synthetic reactions utilized include Keck allylation, Evans asymmetric methylation, Grubbs metathesis and Julia-Kocienski olefination reaction.
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海洋衍生抗真菌药(-)-melearoride A和抗生素(-)- pf1163b的全合成
以两种不同的路线描述了通过其结构中存在的共同骨架合成两种13元大环内酯的灵活的立体选择性和收敛-发散方法,总产率良好。使用的关键合成反应包括Keck烯丙基化、Evans不对称甲基化、Grubbs复分解和Julia Kocienski油化反应。
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来源期刊
SynOpen
SynOpen CHEMISTRY, ORGANIC-
CiteScore
2.30
自引率
4.00%
发文量
35
审稿时长
6 weeks
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