@article { ISI:000260209800002,
	title = {Efficient synthesis of quinoxalines in the ionic liquid 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4) at ambient temperature},
	journal = {Synthetic Communications},
	volume = {38},
	number = {21},
	year = {2008},
	month = {FEB},
	pages = {3601-3612},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>Quinoxaline derivatives have been synthesized in excellent yields using an ionic liquid (IL) (viz., 1-n-butylimidazolium tetrafluoroborate) as a reaction medium as well as promoter from various 1,2-diketones and aryl-1,2-diamines. The process is general for the synthesis of quinoxaline derivatives from aromatic as well as aliphatic-1,2-diketones. The advantages of the present method are ambient reaction temperature, simplicity of operation, high yields of products, the recyclability of the IL, and ecofriendly nature of the reaction medium.</p>},
	keywords = {1, 2-diamines, 2-Diketones, Aryl-1, ionicliquid(IL), quinoxalines},
	issn = {0039-7911},
	doi = {10.1080/00397910802054271},
	author = {Potewar, Taterao M. and Ingale, Sachin A. and Srinivasan, Kumar V.}
}
@article { ISI:000261921400006,
	title = {Proline-catalyzed simple and efficient synthesis of 1,8-dioxo-decahydroacridines in aqueous ethanol medium},
	journal = {Synthetic Communications},
	volume = {39},
	number = {2},
	year = {2009},
	month = {DEC},
	pages = {PII 907127919},
	publisher = {TAYLOR \& FRANCIS INC},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>Proline-catalyzed synthesis of 1,8-dioxo-decahydroacridines is achieved via one-pot, three-component condensation of aromatic aldehydes, cyclic diketone, and aryl amines in aqueous ethanol medium. This method offers the advantages of proceeding in neutral and mild conditions, giving high to excellent yields of acridines with easy workup procedure.</p>},
	keywords = {1, 8-dioxodecahydroacridines, aqueous media, one-pot MCR, Proline},
	issn = {0039-7911},
	doi = {10.1080/00397910802044306},
	author = {Venkatesan, K. and Pujari, Suresh S. and Srinivasan, Kumar V.}
}
