@article { ISI:000228983300063,
	title = {Total synthesis of microcarpalide},
	journal = {Journal of Organic Chemistry},
	volume = {70},
	number = {10},
	year = {2005},
	month = {MAY},
	pages = {4207-4210},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>An efficient, convergent approach for the total synthesis of microcarpalide (1) is described. The synthetic strategy features the Sharpless asymmetric dihydroxylation, regioselective epoxide opening with various nucleophiles such as a lithium acetylide and cuprates derived from the vinyl stannane and the vinyl iodide for the construction of a C7-C8 trans-double bond and Yamaguchi macrolactonization as the key steps.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo050193e},
	author = {Kumar, P and Naidu, SV}
}
