@article { ISI:000258433400008,
	title = {Highly selective approach for the total synthesis of (+)-heliconol A},
	journal = {Tetrahedron-Asymmetry},
	volume = {19},
	number = {13},
	year = {2008},
	month = {JUL},
	pages = {1568-1571},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The total synthesis of heliconol A, a representative of a new class of polyketide-derived hemiketals containing a reduced furanocyclopentane unit, has been achieved via the stereoselective reduction of a ketone, the face selective dihydroxylation, a Sonogashira coupling reaction, and a cis-selective reduction as the key steps. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2008.05.031},
	author = {Mohapatra, Debendra K. and Chatterjee, Bhaskar and Gurjar, Mukund K.}
}
@article { ISI:000263319900006,
	title = {Highly stereoselective approach toward the synthesis of the macrolactone core of amphidinolide W},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {7},
	year = {2009},
	month = {FEB},
	pages = {755-758},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The diastereoselective synthesis of the macrolactone core of amphidinolide W was successfully accomplished using Evans{\textquoteright} asymmetric alkylation, Aldol reaction, Julia-Kocienski olefination, and Kita{\textquoteright}s macrocyclization protocol. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Amphidinolide W, Evans aldol, Evans alkylation, Julia-Kocienski olefination, Kita{\textquoteright}s macrocyclization},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2008.11.088},
	author = {Mohapatra, Debendra K. and Chatterjee, Bhaskar and Gurjar, Mukund K.}
}
