T. Manabe et al., NEW EXAMPLES OF 1,6-HYDROGEN AND 1,7-HYDROGEN TRANSFER PROMOTED BY ANALPHA-SILYL GROUP IN RHODIUM(I)-CATALYZED RADICAL REACTIONS OF ACYCLIC ENEDIYNES, Organometallics, 17(14), 1998, pp. 2942-2944
A rhodium(I) catalyst triggers cycloaromatization of omega-trialkylsil
ylated acyclic enediynes to afford benzosilacycloalkane or vinylsilane
products via 1,6- and/or 1,7-hydrogen transfer, presumably effected b
y radical stabilization by an alpha-silyl moiety, and via a seven and/
or eight-membered rhodacycle intermediate. The addition of a catalytic
amount of dimethyl maleate is essential to obtain, better yields air
the products.