Issue 8, 2011

Highly enantioselective synthesis of cyclic sulfamidates and sulfamidesviarhodium-catalyzed transfer hydrogenation

Abstract

We achieved highly enantioselective synthesis of cyclic 1,2-sulfamidates and -sulfamides viarhodium-catalyzed transfer hydrogenation, and also revealed one-pot preparation of cyclic N-sulfonylimines from α-hydroxy ketones.

Graphical abstract: Highly enantioselective synthesis of cyclic sulfamidates and sulfamidesviarhodium-catalyzed transfer hydrogenation

Supplementary files

Article information

Article type
Communication
Submitted
01 Oct 2010
Accepted
17 Nov 2010
First published
17 Dec 2010

Chem. Commun., 2011,47, 2372-2374

Highly enantioselective synthesis of cyclic sulfamidates and sulfamidesviarhodium-catalyzed transfer hydrogenation

S. A. Lee, S. H. Kwak and K. Lee, Chem. Commun., 2011, 47, 2372 DOI: 10.1039/C0CC04166A

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