Unlike the class cross coupling reactions, the cross electrophile coupling (XEC) reactions are an attractive alternative since they do not require the highly sensitive organometallic reagents.
The electrophile−electrophile cross-coupling of carboxylic acid derivatives and alkylpyridinium salts via C−N bond cleavage is developed. Besides acid chlorides, carboxylic acids were also employed as acylating agents, which enabled us to incorporate acid-sensitive functional groups such as MOM, BOC, and acetal.
Hydrosilylation of alkynes inevitably yields α- and β-isomers of vinyltrialkoxysilanes even with complex ligands and catalysts, limiting its usage in organic synthesis. We report the synthesis of α-vinyltrialkoxysilanes via cross-electrophile C(sp2)–C(sp2) coupling of bromoalkenes.