@article {44199,
	title = {First total synthesis of (+/-)-rhodoconferimide},
	journal = {Synthesis-Stuttgart},
	volume = {50},
	year = {2018},
	month = {FEB},
	pages = {658-662},
	type = {Article},
	abstract = {<p>Starting from vanillin and dimethyl maleate, a concise and efficient racemic total synthesis of the potent antioxidant marine natural product (+/-)-rhodoconferimide has been carried out via the Wittig reaction, catalytic hydrogenation, selective brominations, and imide formation. An appropriate regioselective double bromination of the aromatic ring was a key step in the synthesis.</p>},
	keywords = {(+/-)-rhodoconferimide, Antioxidants, Bromination, Natural products, Total synthesis, Vanillin},
	issn = {0039-7881},
	doi = {10.1055/s-0036-1590944},
	author = {Pandhade, Kailas R. and N. P. Argade}
}
@article {47000,
	title = {Chemoselective ring closure of 4-(3-Methyl-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)butanal leading to pandalizine A},
	journal = {ACS Omega},
	volume = {5},
	year = {2020},
	month = {JAN },
	pages = {859-863},
	type = {Article},
	abstract = {<p>Starting from methylmaleic anhydride, a facile total synthesis of pandalizine A alkaloid is described via the regioselective reduction of methylmaleimide and acid-catalyzed enolization of 4-(3-methyl-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)butanal followed by chemoselective intramolecular dehydrative cyclization as the key steps. It is noteworthy that the analogous model system with an additional beta-methyl group followed an alternative chemoselective intermolecular aldol condensation pathway.</p>
},
	issn = {2470-1343},
	doi = {10.1021/acsomega.9b03760},
	author = {Yadav, Mahesh B. and Pandhade, Kailas R. and Argade, Narshinha P.}
}
