The α-arylation of α-bromo- and α-chloroenones using palladium-catalysed cross-coupling

J. C. Banks; D. Van Mele; C.G. Frost

doi:10.1016/j.tetlet.2006.02.134

The α-arylation of α-bromo- and α-chloroenones using palladium-catalysed cross-coupling

J. C. Banks, D. Van Mele, C.G. Frost

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

23 Citations (SciVal)

Abstract

The palladium-catalysed cross-coupling reaction of various arylboronic acids with α-bromoenones and α-chloroenones offers an operationally simple approach to the synthesis of both cyclic and acyclic α-arylenones.

Original language	English
Pages (from-to)	2863-2866
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	17
DOIs	https://doi.org/10.1016/j.tetlet.2006.02.134
Publication status	Published - 24 Apr 2006

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10.1016/j.tetlet.2006.02.134

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title = "The α-arylation of α-bromo- and α-chloroenones using palladium-catalysed cross-coupling",

abstract = "The palladium-catalysed cross-coupling reaction of various arylboronic acids with α-bromoenones and α-chloroenones offers an operationally simple approach to the synthesis of both cyclic and acyclic α-arylenones. ",

author = "Banks, {J. C.} and {Van Mele}, D. and C.G. Frost",

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AU - Van Mele, D.

AU - Frost, C.G.

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N2 - The palladium-catalysed cross-coupling reaction of various arylboronic acids with α-bromoenones and α-chloroenones offers an operationally simple approach to the synthesis of both cyclic and acyclic α-arylenones.

AB - The palladium-catalysed cross-coupling reaction of various arylboronic acids with α-bromoenones and α-chloroenones offers an operationally simple approach to the synthesis of both cyclic and acyclic α-arylenones.

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UR - http://dx.doi.org/10.1016/j.tetlet.2006.02.134

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

The α-arylation of α-bromo- and α-chloroenones using palladium-catalysed cross-coupling

Abstract

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