Formal Syntheses of (−)-Lepadiformines A, C, and (−)-Fasicularin

Volume: 84, Issue: 9, Pages: 5222 - 5229
Published: Apr 3, 2019
Abstract
Marine tricyclic alkaloids lepadiformine and fasicularin, with a unique perhydropyrrolo[2,1- j]quinoline or perhydropyrido[2,1- j]quinoline framework, were synthesized starting from the B ring of the tricyclic system. This approach includes a highly stereocontrolled diallylation of a cyclic enaminoester and subsequent ring-closing metathesis to construct the A/B ring system, which was transformed into key lactams 32 and 33, and amino alcohol 37....
Paper Details
Title
Formal Syntheses of (−)-Lepadiformines A, C, and (−)-Fasicularin
Published Date
Apr 3, 2019
Volume
84
Issue
9
Pages
5222 - 5229
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