@article { ISI:000325642400017,
	title = {Electrophile induced branching cascade: a powerful approach to access various molecular scaffolds and their exploration as novel anti-mycobacterial agents},
	journal = {Chemical Communications},
	volume = {49},
	number = {86},
	year = {2013},
	month = {SEP},
	pages = {10109-10111},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Herein we report on the Electrophile Induced Branching Cascade (EIBC), a new technique to produce a variety of biologically important molecular scaffolds. Some compounds exhibit excellent activities against Mycobacterium smegmatis.</p>},
	issn = {1359-7345},
	doi = {10.1039/c3cc45289a},
	author = {Patil, Nitin T. and Konala, Ashok and Sravanti, Sudha and Singh, Ashita and Ummanni, Ramesh and Sridhar, Balasubramanian}
}
@article { ISI:000344997100001,
	title = {When gold meets chiral bronsted acid catalysts: extending the boundaries of enantioselective gold catalysis},
	journal = {Chemical Communications},
	volume = {50},
	number = {96},
	year = {2014},
	month = {AUG},
	pages = {15124-15135},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>This review describes the development in the use of Au(I)/Bronsted acid binary catalytic systems to enable an enantioselective transformation in one-pot that cannot be achieved by gold catalysts alone. The examples discussed herein are promising since apart from using chiral ligands there exists a possibility of using chiral Bronsted acids. Clearly, the horizon for enantioselective gold catalysis has been expanded as more options to make the gold-catalyzed reactions enantioselective have become available.</p>},
	issn = {1359-7345},
	doi = {10.1039/c4cc04633a},
	author = {Inamdar, Suleman M. and Konala, Ashok and Patil, Nitin T.}
}
