@article { ISI:000358099300015,
	title = {Enantioselective synthesis of (+)-hygroline and (+)-pseudohygroline via Keck allylation and CBS reduction},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {32},
	year = {2015},
	month = {AUG},
	pages = {4704-4705},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An enantioselective synthesis of (+)-hygroline and (+)-pseudohygroline has been achieved in high optical purity (98\% ee) from readily available 1,4-butanediol. The synthesis strategy employs a Keck allylation, CBS reduction, and Wacker oxidation. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {CBS reduction, Keck allylation, Pyrrolidines, Wacker oxidation},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.06.012},
	author = {Bhoite, Shubhangi P. and Kamble, Rohit B. and Suryavanshi, Gurunath M.}
}
@article { ISI:000350528300022,
	title = {Formal asymmetric synthesis of (2S,4R)-4-hydroxypipecolic acid via Co(III)(salen)-catalyzed two stereocentered HKR of racemic azido epoxide},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {10},
	year = {2015},
	month = {MAR},
	pages = {1263-1265},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient formal synthesis of (2S,4R)-4-hydroxypipecolic acid has been achieved in high optical purity (99\% ee) from readily available benzaldehyde. The strategy employs an iodine-induced intramolecular cyclization of a carbonate and Co-catalyzed Hydrolytic Kinetic Resolution (HKR) of two stereocentered racemic azido epoxide as the key reactions to construct chiral 1,3-amino alcohol functionality. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Azido epoxide, Hydrolytic kinetic resolution, lodocyclization, Piperidine},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.01.113},
	author = {Kamble, Rohit B. and Gadre, Shubhankar Haribhau and Suryavanshi, Gurunath M.}
}
@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}
}
