Organoheteroatom Stannanes in Palladium-Catalyzed Cross-Coupling Reactions with 1-Naphthyl Triflate.

MARIANA BONATERRA, SANDRA E. MARTÍN AND ROBERTO A. ROSSI

ORGANOMETALLICS

AMER CHEMICAL SOC

Año: 2009 vol. 28 p. 933 - 936

0276-7333

We have studied the Pd-catalyzed cross-coupling reaction of organoheteroatom stannanes containing elements of groups 15 (P, As, Sb) and 16 (Se) with 1-naphthyl triflate (3). The stannanes n-Bu3SnZPhn (Z ) P, As, Sb, Se; n ) 1, 2) were synthesized by the reaction of the PhnZ- anion with n-Bu3SnCl. The cross-coupling reactions of these stannanes with 3 in a one-pot procedure afforded the C-heteroatom products PhnZ-1-Naph in good yields for Z ) As, Se (90 and 70% yields, respectively) and moderate yields for Z ) P (51% yield). Only 18% of 1-naphthyldiphenylstibine was obtained. Optimization studies revealed that the combination of LiCl and free PPh3 ligand proved to be particularly effective in enhancing the coupling reaction.