Stable Phosphonium Sila-ylide with Reactivity as a Sila-Wittig Reagent
David Gau, Tsuyoshi Kato, Nathalie Saffon-Merceron, Fernando P. Cossío, Antoine Baceiredo
Abstract
David Gau, Tsuyoshi Kato, Nathalie Saffon-Merceron, Fernando P. Cossío, Antoine Baceiredo
Abstract
The silicon congeners of well-known phosphonium ylides have been considered only as short-lived reactive intermediates. We successfully synthesized a remarkably stable phosphonium sila-ylide. Its X-ray structure reveals a long Si-P bond and a strongly pyramidalized silicon center, indicating a very weak P-Si pi interaction. In addition, it exhibits an alpha,beta-ambiphilic character with a nucleophilic silicon center, similar to its carbon-congener phosphonium ylides. This property of the phosphonium sila-ylide allows its use as a sila-Wittig reagent with carbonyl derivatives.
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The silicon congeners of well-known phosphonium ylides have been considered only as short-lived reactive intermediates. We successfully synthesized a remarkably stable phosphonium sila-ylide. Its X-ray structure reveals a long Si-P bond and a strongly pyramidalized silicon center, indicating a very weak P-Si pi interaction. In addition, it exhibits an alpha,beta-ambiphilic character with a nucleophilic silicon center, similar to its carbon-congener phosphonium ylides. This property of the phosphonium sila-ylide allows its use as a sila-Wittig reagent with carbonyl derivatives.
Key concepts: Phosphonium, Ylide, Wittig reaction, Chemistry, Reagent, Reactivity (psychology), Nucleophile, Medicinal chemistry