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Abstract
A three-step procedure involving Diels-Alder condensation of maleic anhydride with furane, formation of N-substituted imide upon reaction with appropriate diamine and a final retro Diels-Alder regeneration of the maleic carbon-carbon double bond is proposed for an unequivocal synthesis of N-substituted basic maleimides. The novel method is characterized by mild reaction conditions, easy work-up, high yields and no need for additional catalysis.
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- Accepted or Published Version
- DOI:
- Digital Object Identifier (open in new tab) 10.1002/jhet.1651
- License
- Copyright (2013 HeteroCorporation)
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- Category:
- Articles
- Type:
- artykuł w czasopiśmie wyróżnionym w JCR
- Published in:
-
JOURNAL OF HETEROCYCLIC CHEMISTRY
no. 51,
edition 4,
pages 999 - 1003,
ISSN: 0022-152X - Language:
- English
- Publication year:
- 2014
- Bibliographic description:
- Salewska N., Milewska M.: Efficient Method for the Synthesis of Functionalized Basic Maleimides// JOURNAL OF HETEROCYCLIC CHEMISTRY. -Vol. 51, iss. 4 (2014), s.999-1003
- DOI:
- Digital Object Identifier (open in new tab) 10.1002/jhet.1651
- Verified by:
- Gdańsk University of Technology
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