Fluoride catalyzed reaction of silylacetylenes with carbonyl compounds
I Kuwajima, E Nakamura, K Hashimoto
Index: Kuwajima, I.; Nakamura, E.; Hashimoto, K. Tetrahedron, 1983 , vol. 39, # 6 p. 975 - 982
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Citation Number: 63
Abstract
(Phenylethynyl) trimethylsilane undergoes nuclcophilic addition to a variety of carbonyl compounds in the presence of a catalytic amount of fluoride anion to give silylated propargyl alcohol derivatives. The reaction fails with enolizable enones and cyclopentanone. The reaction of bis (trimethylsilyl) acetylene does not stop at the stage of monoadduct, and affords a considerable amount of symmetric bisadduct.(Trimethylsilyl) acetylene attacks 4-t ...
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