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ABSTRACT: This personal account summarizes our recent developments in gold-catalyzed direct substitutions on propargylic (allylic, benzylic) alcohols, with various nucleophiles (and bi-nucleophiles) based on the σ- and/or π-acidity of gold(III) complexes. Synthetic developments are also briefly described.
Beilstein Journal of Organic Chemistry 01/2011; 7:866. · 2.52 Impact Factor
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ABSTRACT: The use N-sulfonyl-protected hydroxylamines as bi-nucleophiles in iron-catalyzed propargylic substitutions allows the selective one-pot synthesis of four classes of substituted isoxazoles or isoxazolines from the same propargylic alcohols (21 examples) by simply tuning the nature of the base.
Chemistry - A European Journal. 01/2010; 16:12207.
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The Journal of Organic Chemistry 01/2010; 75:6050. · 4.45 Impact Factor