@article { ISI:000353085000004,
	title = {Concise enantioselective synthesis of marine macrolide-stagonolide E via organocatalysis},
	journal = {Tetrahedron-Asymmetry},
	volume = {26},
	number = {7},
	year = {2015},
	month = {APR},
	pages = {344-349},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short and efficient enantioselective synthesis of marine macrolide stagonolide E in high enantiomeric purity (98\% ee and 8.5\% overall yield) starting from commercially available raw materials has been achieved. The strategy involves proline catalyzed sequential alpha-aminooxylation and Horner-Wadsworth-Emmons olefination, highly stereoselective Ando{\textquoteright}s cis-olefination, and modified Yamaguchi macrolactonization as the key reaction steps. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2015.03.001},
	author = {Dey, Soumen and Sudalai, Arumugam}
}
