Wei, PH;Ibrahim, AA;Mondal, M;Nalla, D;Harzmann, GD;Tedeschi, FA;Wheeler, KA;Kerrigan, NJ

2010

December

Tetrahedron Letters

Mechanistic studies of the phosphine-catalyzed homodimerization of ketoketenes

Published

13 ()

BETA-LACTONE DIMER ASYMMETRIC-SYNTHESIS TRIVALENT PHOSPHORUS DIMETHYLKETENE DIMERIZATION KETENES RING TRIBUTYLPHOSPHINE DERIVATIVES NMR

51

6690

6694

The mechanism of PBu(3)-catalyzed homodimerization of ketoketenes has been explored and compared with that of the previously reported trialkylphosphite-mediated reactions. NMR studies of the PBu(3)-catalyzed reaction implicated the involvement of tetravalent phosphonium intermediates. Phosphonium intermediates in the catalytic cycle were trapped through reaction with trimethylsilyl chloride and 4-chlorobenzaldehyde, and the resulting products were characterized. A method for the stoichiometric generation of phosphonium enolates was developed as a result of these studies. No evidence was obtained for the involvement of pentacovalent phosphorane intermediates in trialkylphosphine-catalyzed ketoketene homodimerization reactions, in contrast with the mechanism of the trialkylphosphite-mediated homodimerization of dimethylketene. An X-ray crystal structure analysis of methylphenylketene dimer showed that it possesses Z-geometry about the exocyclic olefin. (C) 2010 Elsevier Ltd. All rights reserved.

OXFORD

0040-4039

10.1016/j.tetlet.2010.10.026