@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}
}
@article { ISI:000271841900023,
	title = {First asymmetric total synthesis of aspinolide A},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {50},
	year = {2009},
	month = {DEC},
	pages = {7018-7020},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The first total synthesis of aspinolide A has been achieved using ring-closing metathesis as a key step. The stereogenic centers were generated by means of hydrolytic kinetic resolution (HKR) of racemic epoxides. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Decanolides, epoxides, Hydrolytic kinetic resolution, Ring-closing metathesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2009.09.151},
	author = {Chowdhury, Partha Sarathi and Gupta, Priti and Kumar, Pradeep}
}
