@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 {45424,
	title = { Oxidant-free oxidative gold catalysis: the new paradigm in cross-coupling reactions},
	journal = {Chemical Communications},
	volume = {54},
	year = {2018},
	month = {OCT},
	pages = {11069-11083},
	type = {Article},
	abstract = {<p>The construction of C-C and C-X (X = hetero atom) bonds is the core aspect for the assembly of molecules. In this regard, late transition-metal-catalyzed cross-coupling reactions have retained their dominance for decades. Lately, gold catalysts have been emerging as a reliable contender for such transformations owing to the recent findings that reveal gold{\textquoteright}s potential beyond carbophilic -Lewis acid. The newfound ability of gold to undergo redox transformations under certain circumstances has allowed us to explore gold catalysts as a viable alternative to other late transition-metals for efficient construction of cross-coupled products. This feature article critically presents an overview of all the redox neutral cross-coupling reactions enabled by gold catalysis, which we believe would stimulate further research activities in this promising area.</p>},
	isbn = {1359-7345},
	doi = {10.1039/c8cc05601c},
	author = {Akram, Manjur O. and Banerjee, Somsuvra and Saswade, Sagar S. and Bedi, Vaibhav and Patil, Nitin T.}
}
@article {46317,
	title = {Ortho-oxygenative 1,2-difunctionalization of diarylalkynes under merged gold/organophotoredox relay catalysis},
	journal = {Chemistry-An Asian Journal},
	year = {2019},
	month = {OCT},
	type = {Article; Early Access},
	abstract = {<p>Reported herein is an ortho-oxygenative 1,2-difunctionalization of diarylalkynes under merged gold/organophotoredox catalysis to access highly functionalized 2-(2-hydroxyaryl)-2-alkoxy-1-arylethan-1-ones. Detailed mechanistic studies suggested a relay process, initiating with gold-catalyzed hydroalkoxylation of alkynes, to generate enol-ether followed by a key formal [4+2]-cycloaddition reaction. The successful application of the present methodology was also shown for the synthesis of benzofurans.</p>
},
	keywords = {binary catalyst system, Gold catalysis, organocatalyst, photoredox, synthetic methodology},
	issn = {1861-4728},
	doi = {10.1002/asia.201901275},
	author = {Sancheti, Shashank P. and Akram, Manjur O. and Roy, Rupam and Bedi, Vaibhav and Kundu, Shubhankar and Patil, Nitin T.}
}
