@article { ISI:000358229500042,
	title = {Stereocontrolled synthesis of Hagen{\textquoteright}s gland lactones via iterative proline catalyzed alpha-aminoxylation and oxa-Michael addition reactions},
	journal = {RSC Advances},
	volume = {5},
	number = {75},
	year = {2015},
	month = {JUL},
	pages = {61000-61005},
	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 Hagen{\textquoteright}s gland lactones was achieved using a sequential alpha-aminoxylation/oxa-Michael approach in a highly diastereoselective manner with assignment of relative configurations. This method was found to be applicable to the synthesis of various other isomers of Hagen{\textquoteright}s gland lactones.</p>},
	issn = {2046-2069},
	doi = {10.1039/c5ra10082h},
	author = {Kauloorkar, Shruti Vandana and Jha, Vishwajeet and Jogdand, Ganesh F. and Kumar, Pradeep}
}
