@article { ISI:000271280200036,
	title = {Short synthesis of 3,6-disubstituted N-2-thienyl/aryl-indoles},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {47},
	year = {2009},
	month = {NOV},
	pages = {6562-6566},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short synthetic strategy for 3,6-disubstituted-N-2-thienyl/aryl-indoles, involving reaction of substituted 2,4-difluoro/dichloro-styrene epoxide with substituted 2-formylaminothiophenes or substitued N-formylanilins in the presence of a base followed by treatment with an acid, has been developed The method was applied for the synthesis of a number of indoles with a variety of substitutents at 1, 3, and 6 positions of the indole moiety. (C) 2009 Elsevier Ltd All rights reserved.</p>},
	keywords = {Formylaminothiophene, Gewald synthesis, Indole, Styrene epoxide},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2009.09.049},
	author = {Borate, Hanumant B. and Sawargave, Sangmeshwer P. and Maujan, Suleman R.}
}
