Catalyzed vinylogous Mukaiyama aldol reactions with controlled enantio- and diastereoselectivities

Chemistry. 2009;15(7):1566-9. doi: 10.1002/chem.200802359.

Abstract

In control: A new catalytic vinylogous Mukaiyama aldol reaction provides products with high diastereo- and enantioselectivities (up to 99 % de and ee; see scheme). The relative and absolute stereochemistry of a representative product was rigorously assigned by NMR and CD spectroscopies (measured and calculated), X-ray diffraction, and quantum-chemical calculations.