Enantioselective synthesis of cyclopentenes by (2 + 3) cycloaddition via a 2-carbon phosphonium

03 June 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Herein we report a catalytic enantioselective (2 + 3) cycloaddition in which a vinyl phosphonium intermediate serves as the 2-carbon component. The reaction involves an umpolung umpolung coupling sequence enabled by haloacrylates and chiral enantioenriched phosphepine catalysts. The reaction shows good generality providing access to an array of cyclopentenes, with mechanistic studies supporting stereospecific formation of the vinyl phosphonium intermediate which then undergoes annulation with turn over limiting catalyst elimination. Beyond defining a new approach to cyclopentenes these studies demonstrate that haloacrylates can replace ynoates in reaction designs that require exclusive umpolung coupling at both carbons

Keywords

Enantioselective catalysis
Organophosphines
(2 + 3) cycloaddition
umpolung
cyclopentenes

Supplementary materials

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Experimental procedures and spectral data
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All experimental procedures and characterisation data for novel materials
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