@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:000285311000016,
	title = {Enantio- and diastereocontrolled total synthesis of (+)-strictifolione},
	journal = {European Journal of Organic Chemistry},
	number = {36},
	year = {2010},
	month = {DEC},
	pages = {6993-7004},
	publisher = {WILEY-BLACKWELL},
	address = {COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA},
	abstract = {<p>A concise and practical enantioselective synthesis of (+)-strictifolione has been achieved in high diastereomeric excess using Jacobsen{\textquoteright}s hydrolytic kinetic resolution, proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons olefination of aldehyde and cross olefin/ring-closing metathesis as the key steps.</p>},
	keywords = {Asymmetric synthesis, Hydrolytic kinetic resolution, lactones, Natural products, organocatalysis, Ring-closing metathesis, Total synthesis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201001221},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Naidu, S. Vasudeva and Dhavale, Dilip D.}
}
