@article { ISI:000256839100021,
	title = {Stereoselective synthesis of beta-C-Allyl- and beta-C-propargyl-D-arabinofuranosides},
	journal = {Synthesis-Stuttgart},
	number = {11},
	year = {2008},
	month = {JUN},
	pages = {1783-1787},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The stereoselective synthesis of beta-configured C-allyl- and C-propargyl-D-arabinofuranosides (4,7-anhydro-1,2,3-deoxy-D-gluco-oct-1-enitols and -oct-1-ynitols) was addressed by employing allylation/propargylation of a dialdofuranose under aqueous Barbier reaction conditions and acid-catalyzed furan ring transposition of 5-O-mesyl-manno-oct-7-eno- or 5-O-mesyl-manno-oct-7-ynofuranoside derivatives.</p>},
	keywords = {Allylation, Barbier reaction, C-glycoside, D-mannose, propargylation, Ring transposition},
	issn = {0039-7881},
	doi = {10.1055/s-2008-1067016},
	author = {Ramana, C. V. and Narute, Sachin B. and Gonnade, Rajesh G. and Patil, Rahul S.}
}
@article { ISI:000310947900008,
	title = {Stereospecific synthesis of C-arabinofuranosides and carba-disaccharide analogues of Motif C of cell wall AG complex of Mtb},
	journal = {Tetrahedron Letters},
	volume = {53},
	number = {47},
	year = {2012},
	month = {NOV},
	pages = {6347-6350},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A simple strategy for the synthesis of alpha- and beta-C-arabinofuranosides featuring a furan ring transposition reaction has been developed. A novel double furan ring transposition reaction has proposed and executed for the synthesis of the carba-disaccharide analogue of Motif C of the cell wall AG complex of Mtb. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Arabinose, C-Glycosides, Carba-disaccharide, Cell wall AG complex, Ring transposition},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2012.09.015},
	author = {Patil, Rahul S. and Ahire, Ketan M. and Ramana, C. V.}
}
