2002Journal of the American Chemical SocietyRequires access

A Novel Modified Baylis−Hillman Reaction of Propiolate

Yûji Matsuya, Kousuke Hayashi, Hideo Nemoto

Open publisher page 53 citations

Abstract

A new reaction of propiolates and aldehydes mediated by DABCO analogous to the Baylis-Hillman reaction is described. This reaction provided novel beta-functionalized Baylis-Hillman products and a new methodology for the generation of alkylidene carbene species.

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What this paper is about

A new reaction of propiolates and aldehydes mediated by DABCO analogous to the Baylis-Hillman reaction is described. This reaction provided novel beta-functionalized Baylis-Hillman products and a new methodology for the generation of alkylidene carbene species.

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Available abstract

A new reaction of propiolates and aldehydes mediated by DABCO analogous to the Baylis-Hillman reaction is described. This reaction provided novel beta-functionalized Baylis-Hillman products and a new methodology for the generation of alkylidene carbene species.

Key concepts: DABCO, Chemistry, Baylis–Hillman reaction, Carbene, Organic chemistry, Combinatorial chemistry, Reaction conditions, Adduct

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