1,3-Dibromo 5,5-dimethylhydantoin (DBH): A novel and efficient catalyst for the synthesis of 14-aryl-14H-dibenzo[a, j] xanthenes under solvent-free conditions
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s11426-011-4273-3.pdf
Reference32 articles.
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3. Chibale K, Visser M, Schalkwyk DV, Smith PJ, Saravanamuthu A, Fairlamb AH. Exploring the potential of xanthene derivatives as trypanothione reductase inhibitors and chloroquine potentiating agents. Tetrahedron, 2003, 59(13): 2289–2296
4. Ion RM, Frackowiak D. The incorporation of various porphyrins into blood cells measured via flow cytometry, absorption and emission spectroscopy. Acta Biochim. Pol, 1998, 45(3): 833–845
5. Saint-Ruf G, Hieu HT, Poupelin JP. The effect of dibenzoxanthenes on the paralyzing action of zoxazolamine. Naturwissenschaften, 1975, 62(12): 584–585
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1. One-Pot Synthesis of 14-Aryl-14 H-dibenzo[a,j]xanthene Derivatives Catalyzed by Nano-Alumina Sulfuric Acid Through Solvent-Free Conditions;Letters in Organic Chemistry;2015-12-02
2. Iranian chemist’s efforts to provide various effective methods for the synthesis of xanthenes;Journal of the Iranian Chemical Society;2013-10-11
3. 1,3-Dibromo-5,5-dimethylhydantoin (DBH)/kaolin: An efficient reagent system for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under solvent-free conditions;Chinese Chemical Letters;2012-10
4. 1,3-Dibromo 5,5-dimethylhydantoin (DBH)-Catalyzed Solvent-Free Synthesis of 2-arylbenzimidazoles under Microwave Irradiation;E-Journal of Chemistry;2012
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