Issue 6, 2011

N-Heterocyclic carbene-catalyzed (NHC) three-component domino reactions: highly stereoselective synthesis of functionalized acyclic ε-ketoesters

Abstract

A novel NHC-catalyzed three-component domino strategy to access high functionalized cis-ε-ketoesters with excellent yields (up to 98%) and high stereoselectivities (up to 20 : 1) is documented. The title domino reactions are atom economical and work on a broad range of substrates. The relative stereochemistry could be explained by a cascade crossed-benzoin/oxy-Cope rearrangement/esterification process. The thus-obtained products are of potential synthetic value in the drug research and combinatorial chemistry.

Graphical abstract: N-Heterocyclic carbene-catalyzed (NHC) three-component domino reactions: highly stereoselective synthesis of functionalized acyclic ε-ketoesters

Supplementary files

Article information

Article type
Paper
Submitted
15 Sep 2010
Accepted
29 Nov 2010
First published
30 Nov 2010

Org. Biomol. Chem., 2011,9, 1791-1798

N-Heterocyclic carbene-catalyzed (NHC) three-component domino reactions: highly stereoselective synthesis of functionalized acyclic ε-ketoesters

J. Ma, Y. Huang and R. Chen, Org. Biomol. Chem., 2011, 9, 1791 DOI: 10.1039/C0OB00725K

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