@article { ISI:000358734800021,
	title = {Total synthesis of (+)-petromyroxol via tandem alpha-aminoxylation-allylation and asymmetric dihydroxylation-S(N)2 cyclization approach},
	journal = {RSC Advances},
	volume = {5},
	number = {78},
	year = {2015},
	month = {JUL},
	pages = {63311-63317},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>The total synthesis of (+)-petromyroxol, a tetrahydrofuran (THF)-diol fatty acid, isolated from sea lamprey larvae (Petromyzon marinus) is reported. The present synthesis employs a tandem alpha-aminoxylationallylation, cross metathesis and tandem asymmetric dihydroxylation-S(N)2 cyclization as key steps.</p>},
	issn = {2046-2069},
	doi = {10.1039/c5ra10405j},
	author = {Nookaraju, U. and Kumar, Pradeep}
}
