@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.}
}
