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  • N-Heterocyclic carbene-catalyzed (4+2) cycloaddition/decarboxylation of silyl dienol ethers with α,β-unsaturated acid fluorides.

N-Heterocyclic carbene-catalyzed (4+2) cycloaddition/decarboxylation of silyl dienol ethers with α,β-unsaturated acid fluorides.

Journal of the American Chemical Society (2011-03-12)
Sarah J Ryan, Lisa Candish, David W Lupton
ABSTRACT

Herein we report the first all-carbon N-heterocyclic carbene-catalyzed (4 + 2) cycloaddition. The reaction proceeds with α,β-unsaturated acid fluorides and silyl dienol ethers and produces 1,3-cyclohexadienes with complete diastereocontrol (dr >20:1) while demonstrating a new type of reaction cascade exploiting α,β-unsaturated acyl azoliums.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,3-Cyclohexadiene, contains 0.05% BHT as inhibitor, 97%