@article { ISI:000287801700007,
	title = {Synthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment},
	journal = {Letters in Organic Chemistry},
	volume = {7},
	number = {8},
	year = {2010},
	month = {DEC},
	pages = {657-660},
	publisher = {BENTHAM SCIENCE PUBL LTD},
	address = {EXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES},
	abstract = {<p>The synthesis of C21-C26 fragment of superstolide A, starting from D-glucose diacetonide, involving regioselective ring opening of epoxide by Grignard reagent and regioselective stereospecefic hydroboration oxidation has been described.</p>},
	keywords = {Chiral pool, Potent cytotoxic, Regioselective epoxide opening, Stereoselective hydroboration-oxidation, Superstolide A},
	issn = {1570-1786},
	doi = {10.2174/157017810793811704},
	author = {Pal, Rita and Rahaman, Hasibur and Mohapatra, Debendra K. and Gurjar, Mukund K.}
}
@article { ISI:000304037200008,
	title = {Carbohydrate based total synthesis of xestodecalactone B and C: revision of the absolute configuration},
	journal = {Current Organic Chemistry},
	volume = {16},
	number = {9},
	year = {2012},
	month = {MAY},
	pages = {1159-1168},
	publisher = {BENTHAM SCIENCE PUBL LTD},
	address = {EXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES},
	abstract = {<p>A convergent chiral pool approach for the total synthesis of xestodecalactones B and C was demonstrated in which intramolecular acylation reaction constituted the key step. Synthetic and spectroscopic studies reported herein, suggested that the previously assigned structures of xestodecalactone B and C be interchanged.</p>},
	keywords = {Chiral pool, Hydroboration, Intramolecular acylation, Pinnick oxidation, Revision of absolute configuration, Xestodecalactone B and C},
	issn = {1385-2728},
	author = {Pal, Rita and Rahaman, Hasibur and Gurjar, Mukund K.}
}
