Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction

Walid A. Daoud; Michael L. Turner

doi:10.1246/bcsj.78.367

Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction

Walid A. Daoud
, Michael L. Turner

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

8 Citations (Scopus)

Abstract

An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are useful precursors of 1,4-phenylenevinylene copolymers.

Original language	English
Pages (from-to)	367-369
Journal	Bulletin of the Chemical Society of Japan
Volume	78
Issue number	2
DOIs	https://doi.org/10.1246/bcsj.78.367
Publication status	Published - 15 Feb 2005
Externally published	Yes

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title = "Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction",

abstract = "An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are useful precursors of 1,4-phenylenevinylene copolymers.",

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T1 - Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction

AU - Daoud, Walid A.

AU - Turner, Michael L.

PY - 2005/2/15

Y1 - 2005/2/15

N2 - An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are useful precursors of 1,4-phenylenevinylene copolymers.

AB - An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are useful precursors of 1,4-phenylenevinylene copolymers.

UR - https://www.scopus.com/pages/publications/14744301934

UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-14744301934&origin=recordpage

U2 - 10.1246/bcsj.78.367

DO - 10.1246/bcsj.78.367

M3 - RGC 21 - Publication in refereed journal

SN - 0009-2673

VL - 78

SP - 367

EP - 369

JO - Bulletin of the Chemical Society of Japan

JF - Bulletin of the Chemical Society of Japan

IS - 2

ER -

Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction

Abstract

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