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Synthesis 2008(3): 469-473
DOI: 10.1055/s-2008-1032020
DOI: 10.1055/s-2008-1032020
PAPER
© Georg Thieme Verlag Stuttgart · New York
One-Pot Oxidative Allylation of Morita-Baylis-Hillman Adducts with Allyltrimethylsilane Promoted by Dess-Martin Periodinane/Boron Trifluoride-Diethyl Ether Complex
Further Information
Received
22 October 2007
Publication Date:
10 January 2008 (online)
Publication History
Publication Date:
10 January 2008 (online)

Abstract
Morita-Baylis-Hillman adducts undergo smooth one-pot oxidative conjugate addition with allyltrimethylsilane in the presence of Dess-Martin periodinane/boron trifluoride-diethyl ether complex under mild reaction conditions to afford various homoallylated β-keto ester derivatives in good yields with high 1,4-selectivity.
Key words
Morita-Baylis-Hillman adducts - hypervalent iodine reagents - allylations - conjugate additions - β-keto esters
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