Synthesis of vinylogous amides by gold(I)-catalyzed cyclization of N-boc-protected 6-alkynyl-3,4-dihydro-2H-pyridines

The gold(I)-catalyzed cyclization of N-Boc-protected 6-alkynyl-3,4-dihydro- 2H-pyridines, prepared by the Sonogashira coupling of lactam-derived enol triflates or phosphates, provides vinylogous amides, which are useful intermediates in the synthesis of natural compounds. The Au(I)-catalyzed reaction is carried out with Ph3PAuOTf as a catalyst and proceeds via a 6-endo-dig cyclization to form a vinylgold species that after protodeauration generates a cyclic carbamate intermediate. This intermediate is in most cases not isolated, but the addition of a base to the reaction mixture rapidly and quantitatively delivers the target vinylogous amide. The first synthesis of a natural compound from Sonneratia hainanensis has been accomplished by this approach. © 2013 American Chemical Society.