From Enynyl Esters to Functionalized Polycyclic Derivatives via Cycloisomerization and Post-Functionalization - Sorbonne Université
Journal Articles Synthesis: Journal of Synthetic Organic Chemistry Year : 2016

From Enynyl Esters to Functionalized Polycyclic Derivatives via Cycloisomerization and Post-Functionalization

Abstract

The post-functionalization of ketone products originating from the PtCl2-catalyzed cycloisomerization of enynyl esters is described. Postfunctionalization has been accomplished via diastereoselective alkylation, regioselective cyclopropane opening and regioselective Baeyer Villiger and Beckmann rearrangements to provide functionalized polycycles.
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Dates and versions

hal-01400636 , version 1 (22-11-2016)

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Simon Guelen, Max Blazejak, Virginie Mouriès-Mansuy, Louis Fensterbank. From Enynyl Esters to Functionalized Polycyclic Derivatives via Cycloisomerization and Post-Functionalization. Synthesis: Journal of Synthetic Organic Chemistry, 2016, 48 (19), pp.3199 - 3206. ⟨10.1055/s-0035-1561488⟩. ⟨hal-01400636⟩
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