@article { ISI:000295113200011,
	title = {Stereoselective synthesis of ophiocerins A and C},
	journal = {Tetrahedron-Asymmetry},
	volume = {22},
	number = {11},
	year = {2011},
	month = {JUN},
	pages = {1212-1217},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of ophiocerins A and C has been achieved via a common intermediate. The stereogenic centers were generated by means of Jacobsen{\textquoteright}s hydrolytic kinetic resolution and Sharpless kinetic resolution. (C) 2011 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2011.06.015},
	author = {Show, Krishanu and Gupta, Priti and Kumar, Pradeep}
}
@article {43372,
	title = {Synthesis of ophiocerins A, B and C, botryolide E, decarestrictine O, stagonolide C and 9-epi-stagonolide C employing chiral hexane-1,2,3,5-tetraol derivatives as building blocks},
	journal = {European Journal of Organic Chemistry},
	volume = {27},
	year = {2016},
	month = {SEP},
	pages = {4696-4710},
	abstract = {An organocatalytic approach to the synthesis of (2R,3S)-hexane-1,2,3,5-tetraol (11) derivatives (in the forms of different stereoisomers and bearing different protecting groups) has been developed. The key chiral intermediates 11 were prepared with complete stereocontrol through the proline-catalyzed intermolecular aldol reaction between acetone and d-glyceraldehyde acetonide. The synthetic utility of the intermediates was demonstrated by their transformation into the title hydroxylated pyrans and a variety of unsaturated lactones through standard synthetic protocols.},
	doi = {10.1002/ejoc.201600625},
	author = {Show, Krishanu and Kumar, Pradeep}
}
