@article { ISI:000363828500010,
	title = {Efficient organocatalytic route for asymmetric total synthesis of stagonolide F},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {45},
	year = {2015},
	month = {NOV},
	pages = {6207-6209},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A stereoselective total synthesis of Stagonolide F (98\% ee) is described employing asymmetric alpha-aminooxylation, Jorgensen{\textquoteright}s asymmetric epoxidation, Brown asymmetric allylation, Steglich esterification and ring closing metathesis as key steps. The use of organocatalytic alpha-aminooxylation and Jorgensen{\textquoteright}s asymmetric epoxidation of aldehydes for the introduction of chirality makes this approach more attractive. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {alpha-Aminooxylation, Jorgensens{\textquoteright}s asymmetric epoxidation, Macrolide, Ring-closing metathesis, Total synthesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.09.082},
	author = {Shelke, Anil M. and Suryavanshi, Gurunath}
}
