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Synthesis 2004(7): 1057-1061
DOI: 10.1055/s-2004-822339
DOI: 10.1055/s-2004-822339
PAPER
© Georg Thieme Verlag Stuttgart · New York
Conjugate Additions of α,β-Unsaturated Ketones with Arylzinc Species That Form in situ from Diethylzinc and Arylboronic Acids
Further Information
Received
10 December 2003
Publication Date:
14 April 2004 (online)
Publication History
Publication Date:
14 April 2004 (online)
Abstract
Conjugate addition of α,β-unsaturated ketones with arylzinc species that form in situ from diethylzinc and a series of arylboronic acids by boron-zinc exchange reactions were investigated. 1,4-Addition products were formed in yields of 34-93%.
Keywords
conjugate addition - α,β-unsaturated ketone - arylboronic acid - boron-zinc exchange reaction
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References
Decreasing the amount of Et2Zn led to an incomplete reaction.