Short cuts toward forskolin synthesis: A pentacyclic approach

Massoumé Leclaire; Raymond Levet; Franck Ferreira; Paul-Henri Ducrot; Jean-Yves Lallemand; Louis Ricard

doi:10.1039/B004515M

Journal articles

Short cuts toward forskolin synthesis: A pentacyclic approach

Massoumé Leclaire ^{1, *} Raymond Levet ¹ Franck Ferreira ¹ Paul-Henri Ducrot ² Jean-Yves Lallemand ³ Louis Ricard ³

* Corresponding author

1 DCSO - Laboratoire de synthèse organique

2 Unité de phytopharmacie et médiateurs chimiques

3 DCPH - Laboratoire Hétéroéléments et Coordination

Abstract : A practical synthetic route for the preparation of forskolin intermediate 20 is described. Previously reported lactone 3 was converted to 20 through intermediate 16. The main feature of this work lies in the formation and the cleavage of a tetracyclic intermediate for the stereochemical control in the formation of the tricyclic core of forskolin.

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Submitted on : Tuesday, March 11, 2014 - 1:10:39 PM
Last modification on : Tuesday, March 17, 2020 - 3:28:37 AM

Short cuts toward forskolin synthesis: A pentacyclic approach

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Short cuts toward forskolin synthesis: A pentacyclic approach

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