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Journal ArticleDOI

Practical and Useful Methods for the Enantioselective Reduction of Unsymmetrical Ketones

Vinod K. Singh
- 01 Jan 1992 - 
- Vol. 1992, Iss: 07, pp 605-617
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TLDR
In this article, the recently developed oxazaborolidine catalyzed reduction along with other useful reagents are discussed and compared with other traditional reagents for the reduction of unsymmetrical ketones to optically active alcohols.
Abstract
Enantioselective reduction of unsymmetrical ketones to optically active alcohols is very important in organic synthesis. Catalytic methods have been developed for this process and have not been reviewed previously. In this article the recently developed oxazaborolidine catalyzed reduction along with other useful reagents will be discussed.

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Journal ArticleDOI

The Chemistry of α-Haloketones and Their Utility in Heterocyclic Synthesis

TL;DR: The molecular structures and spectral properties of α-haloketones as well as their syntheses are analyzed and reviewed in this paper, where their reactivity towards oxygen, nitrogen, and sulfur nucleophiles, carboxylic acids, carbon nucleophilic, alkenes, and alkynes are discussed.
Journal ArticleDOI

Chiral pyridine N-oxides: Useful ligands for asymmetric catalysis

TL;DR: In this article, the synthesis and applications in asymmetric catalysis of chiral pyridine Noxide derivatives are reviewed and a review of the main applications of chirality is presented.
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