@article { ISI:000329579900029,
	title = {Dimethyl homophthalates to naphthopyrans: the total synthesis of arnottin I and the formal synthesis of (-)-arnottin II},
	journal = {RSC Advances},
	volume = {4},
	number = {11},
	year = {2014},
	month = {JAN},
	pages = {5531-5535},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A simple and efficient 3-step synthetic protocol has been reported for dimethyl homophthalates to naphthopyrans. Starting from dimethyl 2,3-dimethoxyhomophthalate, a practical synthesis of arnottin I has been described via a base catalyzed mono-alkylation, the selective hydrolysis of an aliphatic ester moiety, two consecutive intramolecular cyclizations and an oxidative aromatization pathway with a very good overall yield. The involved intramolecular acylation followed by an associated enolative lactonization was the decisive step. The synthesis of dihydroarnottin I also completes the formal synthesis of (-)-arnottin II.</p>},
	issn = {2046-2069},
	doi = {10.1039/c3ra45312j},
	author = {Jangir, Ravi and N. P. Argade}
}
@article { ISI:000363220800003,
	title = {Diversity oriented convergent access for collective total synthesis of bioactive multifunctional carbazole alkaloids: synthesis of carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D},
	journal = {Organic Letters},
	volume = {16},
	number = {20},
	year = {2014},
	month = {OCT},
	pages = {5470-5473},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Facile syntheses of imperative carbazole alkaloids carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D have been demonstrated starting from readily available Boc-protected 3-formylindole and dimethyl maleate. The suitably substituted aromatic rings have been designed comprising three/four significant C-C bond forming reactions. The competent Wittig reaction, selective monoalkylations, one-pot regioselective Weinreb amide formation and Boc-deprotection, well designed Grignard reactions, dehydrative intramolecular cyclizations, and Baeyer-Villiger rearrangement of aromatic aldehydes were the main features.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol502721r},
	author = {Markad, Shivaji B. and N. P. Argade}
}
@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}
}
