Issue 7, 2015

Regio- and stereoselective synthesis of benzothiazolo-pyrimidinones via an NHC-catalyzed Mannich/lactamization domino reaction

Abstract

An NHC-catalyzed regio- and stereoselective Mannich/lactamization domino reaction of N-(benzothiazolyl)imines with α-chloroaldehydes has been developed. This new protocol provides a facile approach for the asymmetric synthesis of benzothiazolo-pyrimidinones and a pyrrolo[1,2-a]indolone in moderate to good yields (34–78%) and excellent stereoselectivities (87–99% ee, up to >20 : 1 d.r.).

Graphical abstract: Regio- and stereoselective synthesis of benzothiazolo-pyrimidinones via an NHC-catalyzed Mannich/lactamization domino reaction

Supplementary files

Article information

Article type
Communication
Submitted
30 Oct 2014
Accepted
26 Nov 2014
First published
26 Nov 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 1263-1266

Author version available

Regio- and stereoselective synthesis of benzothiazolo-pyrimidinones via an NHC-catalyzed Mannich/lactamization domino reaction

Q. Ni, X. Song, J. Xiong, G. Raabe and D. Enders, Chem. Commun., 2015, 51, 1263 DOI: 10.1039/C4CC08594A

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