Palladium-catalyzed cross-coupling of allylic carbonates with alkenylfluorosilanes in the absence of fluoride ion

Hayao Matsuhashi; Yasuo Hatanaka; Manabu Kuroboshi; Tamejiro Hiyama

doi:10.1016/0040-4039(95)00082-N

Palladium-catalyzed cross-coupling of allylic carbonates with alkenylfluorosilanes in the absence of fluoride ion

Hayao Matsuhashi, Yasuo Hatanaka, Manabu Kuroboshi, Tamejiro Hiyama

Research output: Contribution to journal › Article › peer-review

32 Citations (Scopus)

Abstract

Alkenylfluorosilanes smoothly underwent cross-coupling reaction with allylic carbonates in the presence of a palladium catalyst andin the absence of fluoride ion to give 1, 4-dienes in good yields with retention of configuration.

Original language	English
Pages (from-to)	1539-1540
Number of pages	2
Journal	Tetrahedron Letters
Volume	36
Issue number	9
DOIs	https://doi.org/10.1016/0040-4039(95)00082-N
Publication status	Published - Feb 27 1995
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/0040-4039(95)00082-N

Cite this

@article{2bd67f1243f74624a575e1a723723734,

title = "Palladium-catalyzed cross-coupling of allylic carbonates with alkenylfluorosilanes in the absence of fluoride ion",

abstract = "Alkenylfluorosilanes smoothly underwent cross-coupling reaction with allylic carbonates in the presence of a palladium catalyst andin the absence of fluoride ion to give 1, 4-dienes in good yields with retention of configuration.",

author = "Hayao Matsuhashi and Yasuo Hatanaka and Manabu Kuroboshi and Tamejiro Hiyama",

year = "1995",

month = feb,

day = "27",

doi = "10.1016/0040-4039(95)00082-N",

language = "English",

volume = "36",

pages = "1539--1540",

journal = "Tetrahedron Letters",

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number = "9",

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T1 - Palladium-catalyzed cross-coupling of allylic carbonates with alkenylfluorosilanes in the absence of fluoride ion

AU - Matsuhashi, Hayao

AU - Hatanaka, Yasuo

AU - Kuroboshi, Manabu

AU - Hiyama, Tamejiro

PY - 1995/2/27

Y1 - 1995/2/27

N2 - Alkenylfluorosilanes smoothly underwent cross-coupling reaction with allylic carbonates in the presence of a palladium catalyst andin the absence of fluoride ion to give 1, 4-dienes in good yields with retention of configuration.

AB - Alkenylfluorosilanes smoothly underwent cross-coupling reaction with allylic carbonates in the presence of a palladium catalyst andin the absence of fluoride ion to give 1, 4-dienes in good yields with retention of configuration.

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UR - http://www.scopus.com/inward/citedby.url?scp=0028912687&partnerID=8YFLogxK

U2 - 10.1016/0040-4039(95)00082-N

DO - 10.1016/0040-4039(95)00082-N

M3 - Article

AN - SCOPUS:0028912687

SN - 0040-4039

VL - 36

SP - 1539

EP - 1540

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 9

ER -

Palladium-catalyzed cross-coupling of allylic carbonates with alkenylfluorosilanes in the absence of fluoride ion

Abstract

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