@article { ISI:000294158700021,
	title = {Intramolecular chemoselective acylation of a suitably substituted isoindole: synthesis of (+/-)-chilenine and (+/-)-deoxychilenine},
	journal = {Synthesis-Stuttgart},
	number = {17},
	year = {2011},
	month = {SEP},
	pages = {2838-2842},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Starting from 3,4-dimethoxyhomophthalic anhydride and 6-bromohomopiperonylamine, concise and efficient syntheses of Chilean berberis products chilenine and deoxychilenine have been demonstrated via partially divergent routes by taking advantage of facile air-oxidation of homophthalimide along with intramolecular chemoselective acylation as the key steps.</p>},
	keywords = {chemoselective acylation, chilenine, deoxychilenine, homophthalic anhydride, isoindole, Total synthesis},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1260140},
	author = {Wakchaure, Prasad B. and N. P. Argade}
}
