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Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013)

Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with... Organocatalysis Maleimides are known to be very good electrophiles, dienophiles, and dipolarophiles. In their Full Paper on page 586 ff., Pankaj Chauhan and Swapandeep Singh Chimni demonstrate that maleimide derivatives can be used as nucleophilic partners in an efficient organocatalytic Morita‐Baylis‐Hillman reaction with isatins catalyzed by β‐isocupreidine. This reaction gives chiral 3‐substituted‐3‐hydroxyoxindoles in high yield and excellent enantioselectivity. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013)

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Publisher
Wiley
Copyright
Copyright © 2013 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201390019
Publisher site
See Article on Publisher Site

Abstract

Organocatalysis Maleimides are known to be very good electrophiles, dienophiles, and dipolarophiles. In their Full Paper on page 586 ff., Pankaj Chauhan and Swapandeep Singh Chimni demonstrate that maleimide derivatives can be used as nucleophilic partners in an efficient organocatalytic Morita‐Baylis‐Hillman reaction with isatins catalyzed by β‐isocupreidine. This reaction gives chiral 3‐substituted‐3‐hydroxyoxindoles in high yield and excellent enantioselectivity.

Journal

Asian Journal of Organic ChemistryWiley

Published: Jul 1, 2013

Keywords: ; ; ; ;

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