@article { ISI:000316095000011,
	title = {Target cum flexibility: simple access to benzofuran conjugated sugar and nucleoside derivatives},
	journal = {Tetrahedron Letters},
	volume = {54},
	number = {14},
	year = {2013},
	month = {APR},
	pages = {1824-1827},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The [Pd]-catalyzed domino process comprising of the coupling of alkynes and o-iodophenol and the subsequent cyclization leading to benzofurans has been successfully applied on the sugar and nucleoside derived alkynes. (C) 2013 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Benzofuran, carbohydrates, cyclization, Nucleoside, Palladium},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2013.01.089},
	author = {Kommagalla, Yadagiri and Srinivas, Kolluru and Ramana, C. V.}
}
@article {44117,
	title = {Total synthesis of propolisbenzofuran B},
	journal = {Organic Letters},
	volume = {19},
	year = {2017},
	month = {DEC},
	pages = {6466-6469},
	type = {Article},
	abstract = {An efficient synthesis of propolisbenzofuran B, which possesses promising anticancer activity, is reported. The key cyclohexanone framework of this tricyclic natural product has been constructed employing a Rh-catalyzed intramolecular olefin hydroacylation. The requisite key olefin intermediate was synthesized by using gold-catalyzed allenyl ether [1,3] O -> C rearrangement.},
	doi = {10.1021/acs.orglett.7b02732},
	author = {Srinivas, Kolluru and Ramana, Chepuri V.}
}
