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Triarylalkenes from the site-selective reductive cross-coupling of benzophenones and aldehydes.

Anna I ArkhypchukNicolas D'ImperioSascha Ott
Published in: Chemical communications (Cambridge, England) (2019)
PhP(Li)TMS converts benzophenones to phosphaalkenes which upon activation under oxidizing, basic conditions react with aromatic aldehydes under the formation of triarylalkenes. The one-pot reaction omits transition metals, proceeds at room temperature and precludes the formation of any homo-coupling products. Systematic substrate variations reveal reactivity patterns that are useful for the identification of ketone/aldehyde combinations that can be coupled in yields up to 80%.
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