@article { ISI:000267070700046,
	title = {Enantioselective total synthesis of (2S,3R,4R)-D-xylo-phytosphingosine from substituted azetidin-2-one},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {26},
	year = {2009},
	month = {JUL},
	pages = {3296-3298},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Enantiomerically pure (2S,3R,4R)-D-xylo phytosphingosine is synthesized in 36\% overall yield in seven steps from known beta-lactam (8) derived from D-mannitol triacetonide. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	keywords = {beta-lactam, Enantioselective synthesis, Sphingosine, Wittig reaction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2009.02.050},
	author = {Pandey, Ganesh and Tiwari, Dharmendra Kumar}
}
