@article { ISI:000264490200029,
	title = {Short total synthesis of (+)-cryptocarya diacetate},
	journal = {Heterocycles},
	volume = {77},
	number = {2},
	year = {2009},
	month = {FEB},
	pages = {945-952},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short synthesis of (+)-cryptocarya diacetate was achieved by employing three component linchpin coupling, diastereoselective reduction of beta-hydroxyketone, and Z-selective HWE reaction as key transformations.</p>},
	keywords = {Brook Rearrangement, cryptocarya diacetate, Diastereoselective Reduction, Horner-Wadswarth-Emmons Reaction, Linchpin coupling},
	issn = {0385-5414},
	doi = {10.3987/COM-08-S(F)107},
	author = {Gurjar, Mukund K. and Raghupathi, Neelarapu and Chorghade, Mukund S.}
}
@article { ISI:000320275600007,
	title = {Desymmetrization approach to the enantiopure syn/anti-1,5-diols via hydrolytic kinetic resolution (hkr) of functionalized meso-bis-epoxides: further elaboration to syn/syn-1,3,5-triols and application to the formal synthesis of cryptocarya diacetate},
	journal = {Advanced Synthesis \& Catalysis},
	volume = {355},
	number = {9},
	year = {2013},
	month = {JUN},
	pages = {1719-1723},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>A new approach has been developed for the synthesis of enantiopure syn/anti-1,5-diols by desymmetrization of functionalized meso-bis-epoxides using hydrolytic kinetic resolution (HKR). The usage of this protocol was demonstrated by converting syn-1,5-diols into syn/syn-1,3,5-triols and its subseqent application to the formal synthesis of cryptocarya diacetate.</p>},
	keywords = {bis-epoxides, cryptocarya diacetate, desymmetrization, stereoselective reduction, synthetic methods},
	issn = {1615-4150},
	doi = {10.1002/adsc.201300098},
	author = {Kumar, Pradeep and Chowdhury, Partha Sarathi and Pandey, Menaka}
}
