@article { ISI:000228575900016,
	title = {Asymmetric total synthesis of eicosanoid},
	journal = {Arkivoc},
	number = {3},
	year = {2005},
	month = {JAN},
	pages = {144-155},
	publisher = {ARKAT USA INC},
	type = {Article},
	address = {C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA},
	abstract = {<p>An asymmetric total synthesis of eicosanoid 4 starting from 2,2- dimethyl-( R)- 1,3- dioxolane-4- carbaldehyde is described. The key steps involved for the synthesis include modified Simmons-Smith cyclopropanation, stereoselective reduction, ring-closing metathesis (RCM) and Nozaki- Hiyama- Kishi coupling reaction.</p>},
	keywords = {cyclopropanation, eicosanoid, lipoxygenase inhibitors, Ring-closing metathesis, Stereoselective},
	author = {Mohapatra, Debendra K. and Yellol, G. S.}
}
@article { ISI:000253170200010,
	title = {Stereoselective synthesis of the C33-C44 fragment of palau{\textquoteright}amide},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {5},
	year = {2008},
	month = {JAN},
	pages = {786-789},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient stereoselective synthesis of the C33-C44 fragment of palau{\textquoteright}amide is described using a Sharpless asymmetric epoxidation, a regioselective nucleophilic ring opening of the epoxide, a Grignard reaction and a Luche stereoselective reduction of a keto compound as the key steps. (C) 2007 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Cytotoxic, Luche{\textquoteright}s stereoselective reduction, palau{\textquoteright}amide, Sharpless asymmetric epoxidation, Stereoselective},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2007.11.200},
	author = {Mohapatra, Debendra K. and Nayak, Sabita}
}
