@article {42843,
	title = {Oxidative intramolecular 1,2-amino-oxygenation of alkynes under Au(I)/Au(III)-catalysis: discovery of pyridinium-oxazole dyad as novel lonic fluorophore},
	journal = {Angewandte Chemie International Edition},
	year = {2016},
	month = {JAN},
	doi = {10.1002/anie.201609335R1},
	author = {Shaikh, Aslam C. and Ranade, Dnyanesh S. and Rajamohanan, Pattuparambil R. and Kulkarni, Prasad P. and Patil, Nitin T.}
}
@article {43360,
	title = {Oxidative intramolecular 1,2-amino-oxygenation of alkynes under Au I /Au III catalysis: discovery of a pyridinium-oxazole dyad as an ionic fluorophore},
	journal = {Angewandte Chemie-International Edition},
	volume = {56},
	year = {2017},
	month = {JAN},
	pages = {757 - 761},
	doi = {10.1002/ange.201609335},
	author = {Shaikh, Aslam C. and Ranade, Dnyanesh Sadanand and Rajamohanan, Pattuparambil R. and Kulkarni, Prasad Padmakar and Patil, Nitin T.}
}
@article {43482,
	title = {Oxidative intramolecular 1,2-amino-oxygenation of alkynes under Au-I/Au-III catalysis: discovery of a pyridinium-oxazole dyad as an ionic fluorophore},
	journal = {Angewandte Chemie-International Edition},
	volume = {56},
	year = {2017},
	month = {JAN},
	pages = {757-761},
	abstract = {Oxidative intramolecular 1,2-amino-oxygenation reactions, combining gold(I)/gold(III) catalysis, is reported. The reaction provides efficient access to a structurally unique ionic pyridinium-oxazole dyad with tunable emission wavelengths. The application of these fluorophores as potential biomarkers has been investigated.},
	doi = {10.1002/anie.201609335},
	author = {Shaikh, Aslam C. and Ranade, Dnyanesh S. and Rajamohanan, Pattuparambil R. and Kulkarni, Prasad P. and Patil, Nitin T.}
}
@article {46349,
	title = {Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams},
	journal = {RSC Advances},
	volume = {9},
	year = {2019},
	month = {SEP },
	pages = {30277-30291},
	type = {Article},
	abstract = {<p>Oxone promoted intramolecular dehydrogenative imino Diels-Alder reaction (Povarov cyclization) of alkyne tethered N-aryl glycine esters and amides has been explored, thus affording biologically significant quinoline fused lactones and lactams. The reaction is simple, scalable, and high yielding (up to 88\%). The method was further extended to prepare biologically important luotonin-A analogues and the quinoline core of uncialamycin.</p>
},
	doi = {10.1039/c9ra06212b},
	author = {More, Devidas A. and Shinde, Ganesh H. and Shaikh, Aslam C. and Muthukrishnan, M.}
}
