@article { ISI:000379493900061,
	title = {Total synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization},
	journal = {RSC Advances},
	volume = {6},
	number = {68},
	year = {2016},
	month = {JUN},
	pages = {63607-63612},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A simple and efficient synthesis of the 14-membered macrolide (-)-(6R,11R,14S)-colletallol was achieved in a highly diastereoselective manner with high overall yield. The stereogenic centre was generated using a proline catalyzed alpha-aminoxylation reaction and the ring was constructed using Yamaguchi protocol.</p>},
	issn = {2046-2069},
	doi = {10.1039/c6ra08484b},
	author = {Kauloorkar, Shruti Vandana and Kumar, Pradeep}
}
