@article { ISI:000239278600023,
	title = {Propargyl glycosides as stable glycosyl donors: anomeric activation and glycoside syntheses},
	journal = {Journal of the American Chemical Society},
	volume = {128},
	number = {30},
	year = {2006},
	month = {AUG},
	pages = {Article No. JA062425C},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	issn = {0002-7863},
	doi = {10.1021/ja062425c},
	author = {Hotha, Srinivas and Kashyap, Sudhir}
}
@article { ISI:000249627100034,
	title = {Propargyl 1,2-orthoesters as glycosyl donors: stereoselective synthesis of 1,2-trans glycosides and disaccharides},
	journal = {Tetrahedron Letters},
	volume = {48},
	number = {37},
	year = {2007},
	month = {SEP},
	pages = {6564-6568},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Propargyl 1,2-orthoesters are identified as glycosyl donors. Various glycosides and disaccharides were synthesized in a stereoselective manner using AuBr3 as the promoter. AuBr3 may activate the alkyne resulting in the formation of a 1,2-dioxolenium ion and also behaves as a Lewis acid to facilitate the attack of the glycosyl acceptor. The versatility of the protocol was demonstrated using a panel of aglycones comprising aliphatic, alicyclic, steroidal and sugar alcohols. (C) 2007 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2007.07.015},
	author = {Sureshkumar, Gopalsamy and Hotha, Srinivas}
}
@article { ISI:000294122000044,
	title = {Propargyl/methyl furanosides as potential glycosyl donors},
	journal = {Chemical Communications},
	volume = {47},
	number = {35},
	year = {2011},
	month = {AUG},
	pages = {9906-9908},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Transfuranosylations are not well studied though many similar studies exist for transpyranosylation; herein, we report that propargyl/methyl D-ribf- and D-lyxf- give only 1,2-trans glycosides whereas D-araf- and D-xylf- result in a mixture of 1,2-trans and 1,2-cis glycosides; observed facts are rationalised by computational studies.</p>},
	issn = {1359-7345},
	doi = {10.1039/c1cc13134f},
	author = {Vidadala, Srinivasa Rao and Gayatri, Gaddamannugu and Sastry, G. Narahari and Hotha, Srinivas}
}
