@article { ISI:000311324100047,
	title = {Pd-Catalyzed imine cyclization: synthesis of antimalarial natural products aplidiopsamine A, marinoquinoline A, and their potential hybrid NCLite-M1},
	journal = {Organic Letters},
	volume = {14},
	number = {22},
	year = {2012},
	month = {NOV},
	pages = {5804-5807},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Palladium-catalyzed cyclization of imines has been developed to construct the extremely rare 3H-pyrrolo[2,3-c]quinoline ring system for diversity oriented first total synthesis of antimalarial marine natural product Aplidiopsamine A as well as synthesis of Marinoquinoline A and potential natural product hybrid NCLite-M1.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol302676v},
	author = {Mahajan, Jyoti P. and Suryawanshi, Yogeshwar R. and Mhaske, Santosh B.}
}
@article {45680,
	title = {Synthesis of methyl-protected (+/-)-chlorizidine A},
	journal = {Organic Letters},
	volume = {19 },
	year = {2017},
	month = {MAY},
	pages = {2774-2776},
	type = {Article},
	chapter = {10 },
	abstract = {The first total synthesis of the methyl-protected (+/-)-chlorizidine A has been achieved in 10 steps. Pd-catalyzed decarboxylative coupling and late-stage oxidation were utilized to, construct the 5H-pyrrolo[2,1-a]isoindol-5-one scaffold. Samarium(II) iodide mediated Reformatsky reaction and intramolecular Mitsunobu reactions were efficiently applied for the synthesis of the 2,3-dihydropyrrolizine ring system. Chlorizidine A is highly prone to degradation; hence, methyl-protected (+/-)-chlorizidine A was prepared.},
	doi = {10.1021/acs.orglett.7b01090},
	author = {Mahajan, Jyoti P. and Mhaske, Santosh B.}
}
