@article { ISI:000245142600010,
	title = {Synthesis of the C19-C34 segment of amphidinolide C},
	journal = {Synlett},
	number = {4},
	year = {2007},
	month = {MAR},
	pages = {567-570},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski{\textquoteright}s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.</p>},
	keywords = {amphidinolide C, Cytotoxic, Nozaki-Hiyama-Kishi coupling, Ring-closing metathesis, Wittig reaction},
	issn = {0936-5214},
	doi = {10.1055/s-2007-967968},
	author = {Mohapatra, Debendra K. and Rahaman, Hasibur and Chorghade, Mukund S. and Gurjar, Mukund K.}
}
@article { ISI:000255342400008,
	title = {Synthesis of the C14-C29 segment of amphidinolide U utilizing a tandem dihydroxylation-S(N)2 cyclization protocol},
	journal = {Synlett},
	number = {6},
	year = {2008},
	month = {APR},
	pages = {837-840},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The synthesis of the C14-C29 subunit of amphidinolide U is described. The key steps include the trans-2,5-disubstituted tetrahydrofurans via a highly diastereoselective and high yielding tandem dihydroxylation-S(N)2 cyclization, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.</p>},
	keywords = {amphidinolide U, Cytotoxic, Nozaki-Hiyama-Kishi coupling, tandem dihydroxylation-S(N)2 cyclization, Wittig reaction},
	issn = {0936-5214},
	doi = {10.1055/s-2008-1042931},
	author = {Mohapatra, Debendra K. and Rahaman, Hasibur}
}
