One-pot reduction of enaminones to syn γ-aminoalcohols can be efficiently performed by lithium borohydride in the presence of cerium chloride as Lewis acid. Selectivities are very good with respect to classical reduction method of these products. © 2002 Elsevier Science Ltd. All rights reserved.
Stereoselective reduction of enaminones to syn γ-aminoalcohols
Procopio A.;
2002-01-01
Abstract
One-pot reduction of enaminones to syn γ-aminoalcohols can be efficiently performed by lithium borohydride in the presence of cerium chloride as Lewis acid. Selectivities are very good with respect to classical reduction method of these products. © 2002 Elsevier Science Ltd. All rights reserved.File in questo prodotto:
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