Literature DB >> 19344136

Vanadium-catalyzed asymmetric epoxidation of allylic alcohols in water.

Andrei V Malkov1, Louise Czemerys, Denis A Malyshev.   

Abstract

Asymmetric V-catalyzed epoxidation of allylic alcohols can be carried out in water with chiral ligands, which incorporate sulfonamide and hydroxamic acid fragments. Furthermore, the reaction, notorious for its ligand-deceleration effect, in water turned into the ligand-accelerated process. By using this aqueous protocol, a range of allylic alcohols were epoxidized with up to 94% ee.

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Year:  2009        PMID: 19344136     DOI: 10.1021/jo900294h

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  5 in total

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Authors:  Phillip A Lichtor; Scott J Miller
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5.  Experimental lineage and functional analysis of a remotely directed peptide epoxidation catalyst.

Authors:  Phillip A Lichtor; Scott J Miller
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  5 in total

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