@article { ISI:000259537800008,
	title = {Short enantioselective synthesis of (+)-L-733,060 via Shi epoxidation of a homoallylic carboxylate},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {40},
	year = {2008},
	month = {SEP},
	pages = {5736-5738},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short and efficient enantioselective synthesis of (+)-L-733,060 in 92\% ee via Shi epoxidation of a homoallylic carboxylate is described. Johnson-Claisen rearrangement was employed to obtain the required carbon backbone, whilst intramolecular reductive O-to-N-ring expansion of a delta-azidolactone was used in the construction of the piperidine moiety. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	keywords = {1, 2-aminoalcohols, 3, 3-sigmatropic rearrangement, asymmetric epoxidation, Lactone},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2008.07.086},
	author = {Emmanuvel, Lourdusamy and Sudalai, Arumugam}
}
