@article { ISI:000373519600016,
	title = {Efficient strategy for the construction of both enantiomers of the octahydropyrroloquinolinone ring system: total synthesis of (+)-aspidospermidine},
	journal = {Organic Letters},
	volume = {18},
	number = {7},
	year = {2016},
	month = {APR},
	pages = {1558-1561},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>An efficient and highly stereoselective intramolecular [3 + 2] cycloaddition of nonstabilized azomethine ylide generated from a designed bicyclic aminal precursor is reported for the synthesis of both (-)- and (+)-octahy-dropyrroloquinolinone. One of the enantiomers is further advanced to accomplish the total synthesis of (+)-aspidospermidine.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.6b00374},
	author = {Pandey, Ganesh and Burugu, Shiva Kumar and Singh, Pushpendra}
}
