@article { ISI:000272089600022,
	title = {Enantioselective synthesis of decarestrictine J},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {51},
	year = {2009},
	month = {DEC},
	pages = {7188-7190},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient total synthesis of decarestrictine J has been achieved using ring-closing metathesis and Yamaguchi esterification as key steps. The stereogenic centres were generated by means of iterative hydrolytic kinetic resolution (HKR) of racemic epoxides. (c) 2009 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Decanolides, epoxides, Hydrolytic kinetic resolution, Ring-closing metathesis, Yamaguchi esterification},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2009.10.035},
	author = {Chowdhury, Partha Sarathi and Gupta, Priti and Kumar, Pradeep}
}
