@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:000282106400009,
	title = {Synthesis of (R)-coniine and (S)-coinicine via organocatalytic alpha-aminoxylation of an aldehyde},
	journal = {Synthesis-Stuttgart},
	number = {18},
	year = {2010},
	month = {SEP},
	pages = {3105-3112},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A short and efficient synthesis of the indolizidine alkaloid (S)-coinicine has been achieved using organocatalytic sequential alpha-aminoxylation and Horner-Wadsworth-Emmons olefination of an aldehyde catalyzed by L-proline. Similarly, a common organocatalytic alpha-aminoxylation route has been developed for the asymmetric synthesis of both (R)-coniine and (S)-coinicine.</p>},
	keywords = {hemlock alkaloids, organocatalysis, Proline, sequential reactions, synthesis},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1257869},
	author = {Kondekar, Nagendra B. and Kumar, Pradeep}
}
