4.6 Article

Transformations of diphenylphosphinothioic acid tertiary amides mediated by directed ortho metallation

期刊

ORGANIC & BIOMOLECULAR CHEMISTRY
卷 10, 期 29, 页码 5647-5658

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob25395j

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资金

  1. Ministerio de Ciencia e Innovacion
  2. FEDER [CTQ2008-117BQU, CTQ2011-27705, MAT2010-15094, PTA-2009-2346-I, CSD2006-015]
  3. Ministerio de Asuntos Exteriores, AECID
  4. Ramon y Cajal program

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ortho-Lithiation of N,N-diisopropyl-P,P-diphenylphosphinothioic amide using n-BuLi in the presence of TMEDA in diethyl ether followed by electrophilic trapping is described as an efficient method for the synthesis of ortho-functionalised derivatives in high yields. The structural modification of the phosphinothioic amide includes C-X (X = P, S, Si, Sn, I) and C-C bond forming reactions with a large variety of electrophiles. Additional applications based on functional group transformations are also reported. They include imine formation, desulfurization and Suzuki cross-coupling reactions on selected compounds.

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