This submission belongs to the session a. General Organic Synthesis of the event The 10th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2006
Citation
A. Navarro-Vázquez, M. Abdollahi-Alibeik, D. Rodríguez, I. Mohammadpoor-Baltork, M. F. Martínez-Esperón, B. H. Yousefi, A. García A. García, C. Saá, D. Domínguez, Novel Synthesis of 1,5-Benzodiazepines Catalyzed by Silica-Supported Dodecatungstophosphoric Acid, in Proceedings of The 10th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2006, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-10-01406
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Novel Synthesis of 1,5-Benzodiazepines Catalyzed by Silica-Supported Dodecatungstophosphoric Acid
A. Navarro-Vázquez 1
M. Abdollahi-Alibeik 1
D. Rodríguez 1
I. Mohammadpoor-Baltork 2
M. F. Martínez-Esperón 1
B. H. Yousefi 3
A. García A. García 1
C. Saá 1
D. Domínguez 1
1. Department of Chemistry, Yazd University, Yazd 89195-741, Iran
2. Department of Chemistry, Isfahan University, Isfahan 81746-73441, Iran
3. Department of Nuclear Medicine, Munich University of Technology, Ismaninger Strasse 22, 81675 München, Deutschland
Abstract
Silica supported 12-tungstophosphoric acid catalyzes efficiently the reaction of o-phenylenediamines with ketones under solvent-free condition to afford the corresponding 1,5-benzodi-azepines in good yields. The catalyst can be recovered by simple filtration and reused.
Keywords
n/a
Towards Enantioselective Electrophilic Trifluoromethylation of β-Keto Esters
Syntheses of new azepane derivatives from monosaccharides