@article { ISI:000273066200048,
	title = {Modular total synthesis of aculeatins A, B, E, F and 6-epi-aculeatins E, F},
	journal = {Tetrahedron},
	volume = {66},
	number = {1},
	year = {2010},
	month = {JAN},
	pages = {390-399},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The total synthesis of aculeatins A, B. E and F confirming the assigned absolute configuration of recently isolated aculeatins E and F is documented. A convergent approach has been designed by the addition of both the terminal units (phenol and side chain) at an advanced stage. The central 1,3,5-triol unit with the requisite stereochemistry was prepared from the commercially available alpha-D-glucoheptonic-gamma-lactone. Selective O-debenzylation during the hydrogenolysis of the diyne intermediate and the one pot phenolic oxidation with concomitant spiroketalization highlight the accomplished total syntheses. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	keywords = {aculeatins, Alkyne-oxirane coupling, Natural products synthesis, Oxidative spiroketalization, Sonogashira coupling},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2009.10.058},
	author = {Ramana, C. V. and Pandey, Sunil Kumar}
}
@article { ISI:000288692000046,
	title = {Totall synthesis of (+/-)-sacidumllignan D},
	journal = {Journal of Organic Chemistry},
	volume = {76},
	number = {7},
	year = {2011},
	month = {APR},
	pages = {2315-2318},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of (+/-)-sacidumlignan D featuring a Zn-mediated Barbier reaction and reverse Wacker oxidation to form the key gamma-lactone, its diastereoselective alpha-methylation followed by reduction cyclization, was documented.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo1025749},
	author = {Pandey, Sunil Kumar and Ramana, C. V.}
}
