@article {47497,
	title = {Stereoselective synthesis of subincanadine alkaloids framework},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {58},
	year = {2019},
	month = {JUN},
	pages = {669-673},
	type = {Article},
	abstract = {Starting from, N-tosyltryptamine and (S)-acetoxysuccinic anhydride, a facile synthesis of (-)-indolizinoindolone has been demonstrated as a basic structural outline of bioactive subincanadine alkaloids. Regioselective Grignard reaction with (S)-acetoxysuccinimide, stereoselective intramolecular cyclization to form (-)-indolizinoindolone skeleton and TiCl4 induced condensation with acetaldehyde for stereoselective generation of exocyclic carbon carbon double bond are the key features.},
	keywords = {(S)-Acetoxysuccinimide, alane reduction, condensation, Grignard reaction, indolizinoindolone, PCC-oxidation, stereoselective Pictet-Spengler cyclization},
	issn = {0376-4699},
	author = {Kalshetti, Manojkumar G. and Argade, Narshinha P.}
}
