Issue 41, 2020

Enantioselective formal synthesis of the marine macrolide (−)-callyspongiolide

Abstract

A short enantioselective synthesis of the macrocyclic core 19 of callyspongiolide, involving a homocrotylboration of aldehyde 4, a Still–Genari olefination, an esterification with alcohol 17, and a ring-closing metathesis, is reported.

Graphical abstract: Enantioselective formal synthesis of the marine macrolide (−)-callyspongiolide

Supplementary files

Article information

Article type
Communication
Submitted
16 Mar 2020
Accepted
03 Apr 2020
First published
06 Apr 2020

Chem. Commun., 2020,56, 5536-5539

Enantioselective formal synthesis of the marine macrolide (−)-callyspongiolide

A. Urbina, N. Llor, M. V. Barbieri, J. Bosch and M. Amat, Chem. Commun., 2020, 56, 5536 DOI: 10.1039/D0CC01978J

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