Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates

Jiro Tsuji; Isao Shimizu; Ichiro Minami; Yukihiro Ohashi

doi:10.1016/S0040-4039(00)85719-6

Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates

Jiro Tsuji, Isao Shimizu, Ichiro Minami, Yukihiro Ohashi

Research output: Contribution to journal › Article

138 Citations (Scopus)

Abstract

Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.

Original language	English
Pages (from-to)	4809-4812
Number of pages	4
Journal	Tetrahedron Letters
Volume	23
Issue number	46
DOIs	https://doi.org/10.1016/S0040-4039(00)85719-6
Publication status	Published - 1982

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ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Cite this

Tsuji, J., Shimizu, I., Minami, I., & Ohashi, Y. (1982). Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates. Tetrahedron Letters, 23(46), 4809-4812. https://doi.org/10.1016/S0040-4039(00)85719-6

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abstract = "Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.",

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AU - Ohashi, Yukihiro

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Access to Document

10.1016/S0040-4039(00)85719-6