@article { ISI:000312607100004,
	title = {Asymmetric synthesis of (+)-stagonolide C and (-)-aspinolide A via organocatalysis},
	journal = {Tetrahedron-Asymmetry},
	volume = {23},
	number = {22-23},
	year = {2012},
	month = {DEC},
	pages = {1534-1541},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new enantioselective synthesis of two important fungal metabolites, (+)-stagonolide C and (-)-aspinolide A, has been described from readily available raw materials. Praline catalyzed asymmetric alpha-aminooxylation and Jorgensen{\textquoteright}s epoxidation of aldehydes are the key reactions employed in the introduction of chirality. The formation of the 10-membered lactone core structure was finally accomplished via Steglich esterification and ring closing metathesis reactions. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2012.10.007},
	author = {Shelke, Anil M. and Rawat, Varun and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
