@article { ISI:000301445700014,
	title = {Carbohydrate-based synthesis of the C13-C22 fragment of amphidinolide X},
	journal = {European Journal of Organic Chemistry},
	number = {9},
	year = {2012},
	month = {MAR},
	pages = {1753-1758},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>A facile carbohydrate-based route was developed for the synthesis of the tetrahydrofuran (C13C22) fragment of amphidinolide X. Starting from L-sorbose, the key reactions followed include the stereoselective synthesis of a quaternary center at C1, BartonMcCombie deoxygenation at C2, Mitsunobu inversion at C3, and chain elongation by a Wittig reaction at C5.</p>},
	keywords = {Cytotoxicity, Macrolides, Mitsunobu inversion, Natural products, Wittig reactions},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201101605},
	author = {Gurjar, Mukund K. and Yellol, Gorakh S. and Mohapatra, Debendra K.}
}
