@article {44452,
	title = {Diastereoselective synthesis of (A{\textpm})- epi-subincanadine C},
	journal = {ACS Omega},
	volume = {3},
	year = {2018},
	month = {MAY},
	pages = {5308-5316},
	type = {Article},
	abstract = {Starting from indolylmaleimide, concise and efficient total synthesis of ({\textpm})-epi-subincanadine C was described via stereoselective Wittig olefination, base-induced selective mono-prenylation, regioselective Grignard reaction, diastereoselective Pictet{\textendash}Spengler cyclization, regioselective oxidative carbon{\textendash}carbon double-bond cleavage, one-pot reductions, and intramolecular cyclization pathway. An attempted synthesis of ({\textpm})-subincanadine C via diastereoselective Grignard addition to the α,β-unsaturated γ-lactam or diastereoselective reduction of a carbon{\textendash}carbon double bond also resulted in yet another route to ({\textpm})-epi-subincanadine C.},
	doi = {10.1021/acsomega.8b00587},
	author = {Kalshetti, Manojkumar and N. P. Argade}
}
