Transformations of diphenylphosphinothioic acid tertiary amides mediated by directed ortho metallation

Org Biomol Chem. 2012 Aug 7;10(29):5647-58. doi: 10.1039/c2ob25395j. Epub 2012 Jun 25.

Abstract

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.