@article { ISI:000245388700011,
	title = {Enantioselective synthesis of (-)-pinellic acid},
	journal = {Tetrahedron Letter},
	volume = {48},
	number = {13},
	year = {2007},
	month = {MAR},
	pages = {2279-2282},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An enantioselective convergent approach toward the total synthesis of pinellic acid 1 from 1,9-nonanediol is described. The synthetic strategy features iterative Sharpless asymmetric dihydroxylation, Sonogashira coupling and Birch reduction. (c) 2007 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2007.01.163},
	author = {Naidu, S. Vasudeva 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.}
}
