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 › peer-review

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

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

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title = "Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates",

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.",

author = "Jiro Tsuji and Isao Shimizu and Ichiro Minami and Yukihiro Ohashi",

year = "1982",

doi = "10.1016/S0040-4039(00)85719-6",

language = "English",

volume = "23",

pages = "4809--4812",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "46",

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T1 - Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates

AU - Tsuji, Jiro

AU - Shimizu, Isao

AU - Minami, Ichiro

AU - Ohashi, Yukihiro

PY - 1982

Y1 - 1982

N2 - 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.

AB - 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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U2 - 10.1016/S0040-4039(00)85719-6

DO - 10.1016/S0040-4039(00)85719-6

M3 - Article

AN - SCOPUS:0000423379

VL - 23

SP - 4809

EP - 4812

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 46

ER -

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

Abstract

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