@article { ISI:000258030400010,
	title = {Total synthesis of (S)-(-)-curvularin: a ring-closing-metathesis-based construction of the macrocyclic framework},
	journal = {Synlett},
	number = {12},
	year = {2008},
	month = {JUL},
	pages = {1801-1804},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A convergent, flexible, and efficient approach to the synthesis of curvularin is described. Key step is the high-yielding macrocyclic ring formation by ring-closing metathesis (RCM) using the Grubbs second-generation catalyst.</p>},
	keywords = {curvularin, Cytotoxic, Pinnick oxidation, Ring-closing metathesis, Wittig reaction},
	issn = {0936-5214},
	doi = {10.1055/s-2008-1078504},
	author = {Mohapatra, Debendra K. and Rahaman, Hasibur and Pal, Rita 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.}
}
