Asymmetric organocatalytic reductions mediated by dihydropyridines

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Asymmetric organocatalytic reductions mediated by dihydropyridines.

Catalytic asymmetric reduction reactions have long been the preserve of the transition metal catalyst. Inspired by the myriad efficient enzyme-catalysed reduction reactions routine in biological systems, chemists have recently begun to design chiral metal-free organocatalysts that employ synthetic dihydropyridine NADH analogues as the hydride source with impressive results. Recent developments ...

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ژورنال

عنوان ژورنال: Organic & Biomolecular Chemistry

سال: 2007

ISSN: 1477-0520,1477-0539

DOI: 10.1039/b711499k