Microwave-assisted Suzuki-Miyaura couplings on α-iodoenaminones

Xin Wang; Brandon J. Turunen; Matthew W. Leighty; Gunda I. Georg

doi:10.1016/j.tetlet.2007.10.078

Microwave-assisted Suzuki-Miyaura couplings on α-iodoenaminones

Xin Wang, Brandon J. Turunen, Matthew W. Leighty, Gunda I. Georg

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

20 Scopus citations

Abstract

A systematic study of α-iodination and subsequent Suzuki-Miyaura couplings between non-attenuated enaminones and a wide range of aromatic boronic acids is reported. The microwave-assisted variant of this transformation furnished the α-arylenaminones in significantly shorter reaction times and slightly improved yields as compared to conventional heating.

Original language	English (US)
Pages (from-to)	8811-8814
Number of pages	4
Journal	Tetrahedron Letters
Volume	48
Issue number	50
DOIs	https://doi.org/10.1016/j.tetlet.2007.10.078
State	Published - Dec 10 2007
Externally published	Yes

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title = "Microwave-assisted Suzuki-Miyaura couplings on α-iodoenaminones",

abstract = "A systematic study of α-iodination and subsequent Suzuki-Miyaura couplings between non-attenuated enaminones and a wide range of aromatic boronic acids is reported. The microwave-assisted variant of this transformation furnished the α-arylenaminones in significantly shorter reaction times and slightly improved yields as compared to conventional heating.",

author = "Xin Wang and Turunen, {Brandon J.} and Leighty, {Matthew W.} and Georg, {Gunda I.}",

year = "2007",

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AU - Turunen, Brandon J.

AU - Leighty, Matthew W.

AU - Georg, Gunda I.

PY - 2007/12/10

Y1 - 2007/12/10

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AB - A systematic study of α-iodination and subsequent Suzuki-Miyaura couplings between non-attenuated enaminones and a wide range of aromatic boronic acids is reported. The microwave-assisted variant of this transformation furnished the α-arylenaminones in significantly shorter reaction times and slightly improved yields as compared to conventional heating.

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