Stereoselective total synthesis of 16-membered macrolide aglycons, leuconolides and maridonolides. Macrocyclic stereocontrol based on conformational analysis of the 16-membered macrolide ring

DOI: 10.1248/cpb.39.2819

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2819 - 2829 (1991)

Update date:2022-09-26

Topics:

Authors:

Nakajima

Matsushima

Yonemitsu

Goto Goto

Osawa Osawa

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Article abstract of DOI:10.1248/cpb.39.2819

Sixteen-membered macrolide aglycons with difrerent oxidation levels, leuconolide A₁ (3a), leuconolide A₃ (3b), midecanolide A₁ (3c), maridonolide 11 (4a), and maridonolide 1 (4b), were synthesized from two carbonolide type

Full text of DOI:10.1248/cpb.39.2819

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