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A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[c,e]azepinones: synthesis and biological evaluation

(2011) JOURNAL OF ORGANIC CHEMISTRY. 76(8). p.2828-2839
Author
Organization
Abstract
An unprecedented microwave-assisted multicomponent strategy has been elaborated for the fast, efficient, and diastereoselective generation of the dibenzo[c,e]azepinone scaffold. The generated compounds were evaluated for their bioactivity.
Keywords
SUZUKI-MIYAURA, ORIENTED ORGANIC-SYNTHESIS, UGI REACTION, DRUG DISCOVERY, AZA-ANALOGS, ONE-POT, 2-IMIDAZOLINES, CHEMISTRY, (-)-STEGANACIN, CYCLOADDITION

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Citation

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MLA
Mehta, Vaibhav Pravinchandra et al. “A Microwave-assisted Diastereoselective Multicomponent Reaction to Access Dibenzo[c,e]azepinones: Synthesis and Biological Evaluation.” JOURNAL OF ORGANIC CHEMISTRY 76.8 (2011): 2828–2839. Print.
APA
Mehta, V. P., Modha, S. G., Ruijter, E., Van Hecke, K., Van Meervelt, L., Pannecouque, C., Balzarini, J., et al. (2011). A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[c,e]azepinones: synthesis and biological evaluation. JOURNAL OF ORGANIC CHEMISTRY, 76(8), 2828–2839.
Chicago author-date
Mehta, Vaibhav Pravinchandra, Sachin G Modha, Eelco Ruijter, Kristof Van Hecke, Luc Van Meervelt, Christophe Pannecouque, Jan Balzarini, Romano VA Orru, and Erik Van der Eycken. 2011. “A Microwave-assisted Diastereoselective Multicomponent Reaction to Access Dibenzo[c,e]azepinones: Synthesis and Biological Evaluation.” Journal of Organic Chemistry 76 (8): 2828–2839.
Chicago author-date (all authors)
Mehta, Vaibhav Pravinchandra, Sachin G Modha, Eelco Ruijter, Kristof Van Hecke, Luc Van Meervelt, Christophe Pannecouque, Jan Balzarini, Romano VA Orru, and Erik Van der Eycken. 2011. “A Microwave-assisted Diastereoselective Multicomponent Reaction to Access Dibenzo[c,e]azepinones: Synthesis and Biological Evaluation.” Journal of Organic Chemistry 76 (8): 2828–2839.
Vancouver
1.
Mehta VP, Modha SG, Ruijter E, Van Hecke K, Van Meervelt L, Pannecouque C, et al. A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[c,e]azepinones: synthesis and biological evaluation. JOURNAL OF ORGANIC CHEMISTRY. 2011;76(8):2828–39.
IEEE
[1]
V. P. Mehta et al., “A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[c,e]azepinones: synthesis and biological evaluation,” JOURNAL OF ORGANIC CHEMISTRY, vol. 76, no. 8, pp. 2828–2839, 2011.
@article{2045521,
  abstract     = {An unprecedented microwave-assisted multicomponent strategy has been elaborated for the fast, efficient, and diastereoselective generation of the dibenzo[c,e]azepinone scaffold. The generated compounds were evaluated for their bioactivity.},
  author       = {Mehta, Vaibhav Pravinchandra and Modha, Sachin G and Ruijter, Eelco and Van Hecke, Kristof and Van Meervelt, Luc and Pannecouque, Christophe and Balzarini, Jan and Orru, Romano VA and Van der Eycken, Erik},
  issn         = {0022-3263},
  journal      = {JOURNAL OF ORGANIC CHEMISTRY},
  keywords     = {SUZUKI-MIYAURA,ORIENTED ORGANIC-SYNTHESIS,UGI REACTION,DRUG DISCOVERY,AZA-ANALOGS,ONE-POT,2-IMIDAZOLINES,CHEMISTRY,(-)-STEGANACIN,CYCLOADDITION},
  language     = {eng},
  number       = {8},
  pages        = {2828--2839},
  title        = {A microwave-assisted diastereoselective multicomponent reaction to access dibenzo[c,e]azepinones: synthesis and biological evaluation},
  url          = {http://dx.doi.org/10.1021/jo200251q},
  volume       = {76},
  year         = {2011},
}

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