@article { ISI:000255698500020,
	title = {Total synthesis and determination of relative and absolute configuration of multiplolide A},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {10},
	year = {2008},
	month = {MAY},
	pages = {3817-3822},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A flexible approach for total syntheses of possible multiplolide A diastereomers establishing the relative and absolute configuration is documented. The adopted strategy features ring-closing metathesis (RCM) as the key reaction and screening of a set of substrates for the feasibility of RCM in general and for the requisite E-configuration of ring olefin in particular. Selective protecting groups manipulation prior to the assembly of the central macrocyclic core was instrumental in installing the epoxide functionality on a fully deprotected nonenolide at the end of the synthesis.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo7027568},
	author = {Ramana, C. V. and Khaladkar, Tushar P. and Chatterjee, Soumitra and Gurjar, Mukund K.}
}
