@article { ISI:000258030400010,
	title = {Total synthesis of (S)-(-)-curvularin: a ring-closing-metathesis-based construction of the macrocyclic framework},
	journal = {Synlett},
	number = {12},
	year = {2008},
	month = {JUL},
	pages = {1801-1804},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A convergent, flexible, and efficient approach to the synthesis of curvularin is described. Key step is the high-yielding macrocyclic ring formation by ring-closing metathesis (RCM) using the Grubbs second-generation catalyst.</p>},
	keywords = {curvularin, Cytotoxic, Pinnick oxidation, Ring-closing metathesis, Wittig reaction},
	issn = {0936-5214},
	doi = {10.1055/s-2008-1078504},
	author = {Mohapatra, Debendra K. and Rahaman, Hasibur and Pal, Rita and Gurjar, Mukund K.}
}
@article { ISI:000271055100016,
	title = {Stereoselective synthesis of the densely functionalized C1-C9 fragment of amphidinolides C and F},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {46},
	year = {2009},
	month = {NOV},
	pages = {6276-6279},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The synthesis of the C1-C9 subunit of amphidinolides C and F is described. Key steps include tandem Sharpless asymmetric dihydroxylation-S(N)2 cyclization reaction, Lewis acid-mediated epoxide opening, Wittig reaction, and Wacker oxidation. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Amphidinolide C and F, Cytotoxic, Tandem dihydroxylation-S(N)2, Wacker oxidation, Wittig reaction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2009.09.001},
	author = {Mohapatra, Debendra K. and Dasari, Pavankumar and Rahaman, Hasibur and Pal, Rita}
}
