Abstract
Pure organic: The synthesis of tetrasubstituted furans often involves transition-metal catalysis or metal-halogen exchange reactions. A new approach to these heterocycles employs the Feist-Bénary addition-elimination process using nitroallylic acetates and 1,3-dicarbonyls (see scheme; X=C, O).
Original language | English |
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Pages (from-to) | 688-691 |
Number of pages | 4 |
Journal | Chemistry - An Asian Journal |
Volume | 7 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2012 Apr |
Keywords
- addition
- elimination
- heterocycles
- synthetic methods
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
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Dive into the research topics of 'Efficient synthesis of tetrasubstituted furans from nitroallylic acetates and 1,3-dicarbonyl/α-activating ketones by Feist-Bénary addition-elimination'. Together they form a unique fingerprint.Datasets
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CCDC 853124: Experimental Crystal Structure Determination
Huang, W. (Creator), Chen, Y. (Creator) & Chen, K. (Creator), Unknown Publisher, 2012
DOI: 10.5517/ccxmr4d, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccxmr4d&sid=DataCite
Dataset
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CCDC 853540: Experimental Crystal Structure Determination
Huang, W. (Creator), Chen, Y. (Creator) & Chen, K. (Creator), Unknown Publisher, 2012
DOI: 10.5517/ccxn5k8, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccxn5k8&sid=DataCite
Dataset
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CCDC 853123: Experimental Crystal Structure Determination
Huang, W. (Creator), Chen, Y. (Creator) & Chen, K. (Creator), Unknown Publisher, 2012
DOI: 10.5517/ccxmr3c, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccxmr3c&sid=DataCite
Dataset