@article { ISI:000277129300005,
	title = {Facile synthesis of N-substituted maleimides},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {49},
	number = {4},
	year = {2010},
	month = {APR},
	pages = {487-488},
	publisher = {COUNCIL SCIENTIFIC \& INDUSTRIAL RES},
	address = {ANUSANDHAN BHAWAN, 2 RAFI MARG, NEW DELHI, 110001, INDIA},
	abstract = {<p>A simple and efficient method for the synthesis of N-substituted malemides from the corresponding maleamie acids under the phase transfer catalysis has been described</p>},
	keywords = {Maleamic acids, maleimides, phase transfer catalysis, synthesis},
	issn = {0376-4699},
	author = {Deshpande, Sunita R. and Maybhate, Shailaja P. and Likhite, Anjali P. and Chaudhary, Preeti M.}
}
@article { ISI:000359956500020,
	title = {First regioselective iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1,2,4-triazoles},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {36},
	year = {2015},
	month = {SEP},
	pages = {5140-5144},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The regioselective iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1,2,4-triazoles is described for the first time. The iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1,2,4-triazoles using molecular iodine afforded diiodo-compound which on Cul-catalyzed intramolecular C-N coupling reaction gave six-membered 2-aryl-51141,2,4]triazolo[5,1-b][1,3]thiazines, whereas, the five membered 3-aryl-5,6-dihydrothiazolo[2,3-c][1,2,4]triazoles were obtained exclusively when the iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1,2,4-triazoles was carried out using NIS. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Iodocyclization, Regloselective, Thiazine, Triazole},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.07.006},
	author = {Rode, Navnath D. and Sonawane, Amol D. and Garud, Dinesh R. and Joshi, Rohini R. and Joshi, Ramesh A. and Likhite, Anjali P.}
}
