@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:000341070100010,
	title = {Synthesis of chenopanone},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {53},
	number = {8},
	year = {2014},
	month = {AUG},
	pages = {1140-1142},
	publisher = {COUNCIL SCIENTIFIC \& INDUSTRIAL RES},
	address = {ANUSANDHAN BHAWAN, 2 RAFI MARG, NEW DELHI, 110001, INDIA},
	abstract = {<p>Starting from glyoxalic acid, a facile three step approach to chenopanone has been described utilizing the Barbier reaction as a key step.</p>},
	keywords = {acid hydrolysis, Barbier reaction, chenopanone, condensation, Glyoxalic acid, isovaleraldehyde, synthesis},
	issn = {0376-4699},
	author = {Deore, Prashant S. and N. P. Argade}
}
