Tetrahedron Letters p. 3279 - 3282 (1999)
Update date:2022-08-03
Topics:
Dinon, Franceses
Richards, Elinor
Murphy, Patrick J.
Hibbs, David E.
Hursthouse, Michael B.
Malik, K. M. Abdul
The secondary amine mediated Baylis-Hillman reaction has been found to proceed via a tandem Michael addition/intramolecular aldol followed by a slow elimination step; it was also observed that similar processes can be effected using phosphines and thiols as mediators.
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