@article {43359,
	title = {Catalytic enantioselective aza-piancatelli rearrangement},
	journal = {Synlett},
	volume = {28},
	year = {2017},
	month = {JUN},
	pages = {1096-1100},
	type = {Article},
	abstract = {The design and development of an enantioselective aza-Piancatelli rearrangement reaction are described. In the presence of a chiral phosphoric acid catalyst, furylcarbinols react with anilines to afford highly functionalized cyclopentenones with excellent diastereo-and enantioselectivities. The process was shown to be scalable, and up to 1 gram of starting material could be employed under mild reaction conditions.},
	doi = {10.1055/s-0036-1558952},
	author = {Gade, Amol B. and Patil, Nitin T.}
}
@article {44374,
	title = {Catalytic enantioselective 1,3-alkyl shift in alkyl aryl ethers: efficient synthesis of optically active 3,3 {\textquoteright}-diaryloxindoles},
	journal = {Angewandte Chemie-International Edition},
	volume = {57},
	year = {2018},
	month = {MAY},
	pages = {5735-5739},
	abstract = {Reported is the first organocatalytic asymmetric 1,3-alkyl shift in alkyl aryl ethers for the synthesis of chiral 3,3{\textquoteright}-diaryloxindoles using a chiral Bronsted acid catalyst. Preliminary results showed that each enantiomer of the 3,3{\textquoteright}-diaryloxindole, and a racemic mixture, showed different antiproliferative activities against HeLa cell lines by using an MTT assay.},
	doi = {10.1002/anie.201801650},
	author = {Gade, Amol B. and Bagle, Pradip N. and Shinde, Popat S. and Bhardwaj, Vipin and Banerjee, Subhrashis and Chande, Ajit and Patil, Nitin T.}
}
