@article { ISI:000358370700007,
	title = {Identifying solid luminogens through gold-catalysed intramolecular hydroarylation of alkynes},
	journal = {European Journal of Organic Chemistry},
	number = {22},
	year = {2015},
	month = {AUG},
	pages = {4860-4867},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {POSTFACH 101161, 69451 WEINHEIM, GERMANY},
	abstract = {<p>The identification of a new class of luminogens based on pyrrolo-quinoxaline embedded coumarin (PQC) structures is reported. The reaction relies on the gold-catalyzed hydroarylation reaction of appropriately substituted aryl alkynoates that produces molecules that exhibit solvatochromism and aggregation-induced emission enhancement (AIEE) phenomena. The application of PQCs for live cell imaging has also been demonstrated.</p>},
	keywords = {Cell imaging, Dyes/pigments, fluorescence, Gold, Luminescence, Solvatochromism},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201500503},
	author = {Shaikh, Aslam C. and Shalini, S. and Vaidhyanathan, Ramanathan and Mane, Manoj V. and Barui, Ayan Kumar and Patra, Chitta Ranjan and Venkatesh, Yeduru and Bangal, Prakriti Ranjan and Patil, Nitin T.}
}
@article { ISI:000350116200014,
	title = {Robustness screen in enantioselective catalysis enabled generation of enantioenriched heterocyclic scaffolds in one pot},
	journal = {Chemistry-A European Journal},
	volume = {21},
	number = {9},
	year = {2015},
	month = {FEB},
	pages = {3580-3584},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>Enantioselective catalysis has emerged as a powerful synthetic paradigm and has accelerated the development of new methods to make diverse chiral molecules. Generally, these reactions are very sensitive to the steric and electronic environment present in the catalyst as well as the substrates. With this scenario, the presence of an additional component in the reaction mixture is expected to add complexity in achieving the enantioselective variants. Herein, we report that various enantioenriched molecules could be obtained from multiple starting materials in one pot. The reaction of aminoaromatics A with alkynols B-1, B-2, B-3...B-n with a Au-I/chiral BrOnsted acid catalyst afforded AB(1)*, AB(2)*, AB(3)*...AB(n)*; while, the reaction of alkynols B with aminoaromatics A(1), A(2), A(3)...A(n) under the same reaction conditions gave A(1)B*, A(2)B*, A(3)B*...A(n)B*.</p>},
	keywords = {chiral Bronsted acid, Enantioselectivity, Gold, molecular scaffolds, robustness screen},
	issn = {0947-6539},
	doi = {10.1002/chem.201406045},
	author = {Bagle, Pradip N. and Shinde, Valmik S. and Patil, Nitin T.}
}
