Abstract
Acyl ketenes formed during thermal decompositions of 5-acyl-2,2-dimethyl-1,3-dioxa-4,6-diones undergo stereoselective [2+2] cycloaddition to chiral aldimines. We report the first example of optically active 3-acyl-β-lactams formation from Meldrum’s acid derivatives.
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- Accepted or Published Version
- DOI:
- Digital Object Identifier (open in new tab) 10.1039/C6NJ00884D
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- Copyright (2016 Royal Society of Chemistry)
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- Category:
- Articles
- Type:
- artykuł w czasopiśmie wyróżnionym w JCR
- Published in:
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NEW JOURNAL OF CHEMISTRY
no. 40,
edition 8,
pages 6546 - 6549,
ISSN: 1144-0546 - Language:
- English
- Publication year:
- 2016
- Bibliographic description:
- Zakaszewska A., Najda-Mocarska E., Makowiec S.: The stereoselective formation of β-lactams with acyl ketenes generated from 5-acyl-Meldrum's acids// NEW JOURNAL OF CHEMISTRY. -Vol. 40, iss. 8 (2016), s.6546-6549
- DOI:
- Digital Object Identifier (open in new tab) 10.1039/c6nj00884d
- Verified by:
- Gdańsk University of Technology
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