@article { ISI:000264648900011,
	title = {Stereoselective synthesis of (+)-isoindolo-beta-carboline},
	journal = {Tetrahedron-Asymmetry},
	volume = {20},
	number = {2},
	year = {2009},
	month = {FEB},
	pages = {220-224},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Starting from homophthalic anhydride and (S)-tryptophan, the stereoselective synthesis of (+)-isoindolo-beta-carboline has been described via the corresponding homophthalimide, its chemoselective oxidative ring contraction, and the intramolecular dehydrative ring closure followed by a geometry-specific demethoxycarbonylation. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2009.01.001},
	author = {Wakchaure, Prasad B. and Puranik, Vedavati G. and N. P. Argade}
}
