@article { ISI:000243707700006,
	title = {General and efficient route to 3 {\textquoteleft}-deoxy-3 {\textquoteleft}-N-, S-, and C-substituted altropyranosyl thymines from 2{\textquoteright},3{\textquoteright}-O-anhydro-mannopyranosylthymine},
	journal = {Tetrahedron},
	volume = {63},
	number = {3},
	year = {2007},
	month = {JAN},
	pages = {602-608},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient route to 1-(2,3-O-anhydro-4,6-O-phenylmethylene{\textendash}D-mannopyranosyl) thymine from 1,2,4,6-tetra-O-acetyl-3-O-tosyl-beta-D-glucopyranose has been devised. This newly synthesized epoxide is opened up regioselectively at the C-3{\textquoteright}-position by N-, S-, and C-nucleophiles to afford a wide range of new 3-deoxy-3{\textquoteright}-substituted altropyranosyl thymines. (c) 2006 Published by Elsevier Ltd.</p>},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2006.11.025},
	author = {Deshpande, Sachin G. and Pathak, Tanmaya}
}
