@article { ISI:000231294400029,
	title = {Stereospecific route to 5,11-methanomorphanthridine alkaloids via intramolecular 1,3-dipolar cycloaddition of nonstabilized azomethine ylide: Formal total synthesis of (+/-)-pancracine},
	journal = {Organic Letters},
	volume = {7},
	number = {17},
	year = {2005},
	month = {AUG},
	pages = {3713-3716},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>[GRAPHICS] The core structure of the complex pentacyclic 5,11-methanomorphanthridine alkaloids is constructed stereospecifically in one step employing an intramolecular [3 + 2]-cycloaddition of nonstabilized azomethine ylide as the key step. The strategy is demonstrated by accomplishing the formal total synthesis of (+/-)-pancracine.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol051321o},
	author = {Pandey, Ganesh and Banerjee, Prabal and Kumar, Ravindra and Puranik, Vedavati G.}
}
