@article { ISI:000283834100025,
	title = {Organocatalytic route to the synthesis of lactone moiety of compactin and mevinolin},
	journal = {Tetrahedron Letters},
	volume = {51},
	number = {44},
	year = {2010},
	month = {NOV},
	pages = {5838-5839},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of lactone moiety of compactin has been achieved. The stereogenic centers were generated by means of iterative proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination of aldehydes. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Aminoxylation, Compactin, Lactone, organocatalysis, Proline},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.08.093},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Dhavale, Dilip D.}
}
@article { ISI:000300047600017,
	title = {Organocatalytic stereoselective synthesis of passifloricin A},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {10},
	number = {9},
	year = {2012},
	month = {DEC},
	pages = {1820-1825},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>The enantioselective synthesis of passifloricin A has been achieved in high diastereomeric excess. The 1,3-polyol moiety was constructed by iterative proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination of aldehydes while the synthesis of lactone moiety was achieved by ring-closing metathesis (RCM).</p>},
	issn = {1477-0520},
	doi = {10.1039/c2ob06711k},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Dhavale, Dilip D.}
}
