@article {43656,
	title = {Diastereoselective synthesis of chiral 2,3-disubstituted lndolines via formal [3+2]-cycloaddition of arynes with gamma-amino-alpha,beta-unsaturated esters},
	journal = {Journal of Organic Chemistry},
	volume = {82},
	year = {2017},
	month = {JUN},
	pages = {5940-5946},
	chapter = {5940-5946},
	abstract = {A one step formal [3+2]-annulation protocol for the synthesis of 2,3-disubstituted indolines is described. The in situ generated aryne acts as a two-atom component, and gamma-amino-alpha,beta-unsaturated esters acting as a three-atom component to construct indoline units in a highly regio- and diastereoselective manner with yields ranging from 63 to 80\%.},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.7b00439},
	author = {Aher, Ravindra D. and Suryavanshi, Gurunath M. and Sudalai, Arumugam}
}
