@article {44043,
	title = {Total synthesis of bioactive canthine alkaloid cordatanine comprising in situ double oxidative aromatization of tetrahydrocarbazole},
	journal = {ACS Omega},
	volume = {2},
	year = {2017},
	month = {JUL},
	chapter = {3945-3950},
	abstract = {<p><span style="color: rgb(80, 80, 80); font-family: NexusSan, Arial, Georgia, sans-serif, serif; font-size: 16px;">Starting from tryptamine and methoxymaleic anhydride, concise and efficient total synthesis of cordatanine has been accomplished via regioselective reduction of methoxymaleimide, acid-catalyzed intramolecular cyclization of the formed lactamol, in situ stepwise oxidations leading to aromatization, and intramolecular cyclization with the exchange of N-regioselectivity. An attempted synthesis of regioisomeric natural product zanthochilone has been described in brief with reversal of reduction selectivity.\&nbsp;</span></p>},
	issn = {2470-1343},
	doi = {10.1021/acsomega.7b00609},
	author = {Shelar, S. V. and N. P. Argade}
}
