@article {42863,
	title = {Relay catalytic branching cascade: technique to access diverse molecular scaffolds},
	journal = {Angewandte Chemie International Edition},
	volume = {52},
	year = {2013},
	month = {JAN},
	pages = {2251-2255},
	doi = {10.1002/anie.201208738},
	author = {Patil, Nitin T. and Shinde, Valmik S. and Sridhar, Balasubramanian}
}
@article { ISI:000358349700002,
	title = {Enantioselective cooperative catalysis},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {13},
	number = {30},
	year = {2015},
	month = {JUN},
	pages = {8116-8162},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>In recent years, enantioselective cooperative catalytic reactions, wherein two catalysts work simultaneously to form products which cannot be obtained by the use of a single catalyst alone, have attracted considerable attention. This review focuses on this emerging field, with particular emphasis on mechanistic aspects, which will help readers to understand the role of each catalyst.</p>},
	issn = {1477-0520},
	doi = {10.1039/c5ob00986c},
	author = {Inamdar, Suleman M. and Shinde, Valmik S. and Patil, Nitin T.}
}
@article {42859,
	title = {Gold(I)/chiral br{\o}nsted acid catalyzed enantioselective hydroamination-hydroarylation of alkynes: effect of remote hydroxyl group in the reactivity and enantioselectivity},
	journal = {Chemistry - A European Journal},
	volume = {21},
	year = {2015},
	month = {JAN},
	pages = {975-979},
	doi = {10.1002/chem.201405061},
	author = {Shinde, Valmik S. and Mane, Manoj V. and Vanka, Kumar and Mallick, Arijit 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.}
}
