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Issue 11, 2013
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One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide

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Abstract

A one-pot cross double-Mannich reaction of acetaldehyde was developed, and densely functionalized 1,3-diamines were obtained as a single stereoisomer by use of axially chiral amino sulfonamide (S)-1 as catalyst. Using this catalyst, the one-pot Mannich reaction–aminoxylation was also realized.

Graphical abstract: One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide

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Publication details

The article was received on 21 Nov 2012, accepted on 14 Dec 2012 and first published on 17 Dec 2012


Article type: Communication
DOI: 10.1039/C2CC38370E
Citation: Chem. Commun., 2013,49, 1118-1120

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    One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide

    T. Kano, R. Sakamoto, Y. Yamaguchi, K. Itoh and K. Maruoka, Chem. Commun., 2013, 49, 1118
    DOI: 10.1039/C2CC38370E

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