Mechanistic study of gold(I)-catalyzed intermolecular hydroamination of allenes.

نویسندگان

  • Z Jane Wang
  • Diego Benitez
  • Ekaterina Tkatchouk
  • William A Goddard
  • F Dean Toste
چکیده

The intermolecular hydroamination of allenes occurs readily with hydrazide nucleophiles, in the presence of 3-12% Ph(3)PAuNTf(2). Mechanistic studies have been conducted to establish the resting state of the gold catalyst, the kinetic order of the reaction, the effect of ligand electronics on the overall rate, and the reversibility of the last steps in the catalytic cycle. We have found the overall reaction to be first order in gold and allene and zero order in nucleophile. Our studies suggest that the rate-limiting transition state for the reaction does not involve the nucleophile and that the active catalyst is monomeric in gold(I). Computational studies support an "outersphere" mechanism and predict that a two-step, no intermediate mechanism may be operative. In accord with this mechanistic proposal, the reaction can be accelerated with the use of more electron-deficient phosphine ligands on the gold(I) catalyst.

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عنوان ژورنال:
  • Journal of the American Chemical Society

دوره 132 37  شماره 

صفحات  -

تاریخ انتشار 2010