@article { ISI:000348510400004,
	title = {Catalyst-dependent selectivity in the relay catalytic branching cascade},
	journal = {Chemistry-A European Journal},
	volume = {21},
	number = {6},
	year = {2015},
	month = {FEB},
	pages = {2319-2323},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>The synthesis of small organic molecules as probes for discovering new therapeutic agents has been an important aspect of chemical biology. One of the best ways to access collections of small molecules is to use various techniques in diversity-oriented synthesis (DOS). Recently, a new form of DOS, namely relay catalytic branching cascades (RCBCs), has been introduced, wherein a common type of starting material reacts with several scaffold-building agents (SBAs) to obtain structurally diverse molecular scaffolds under the influence of catalysts. Herein, the RCBC reaction of a common type of substrate with SBAs is reported to give two different types of molecular scaffolds and their formation is essentially dependent on the type of catalyst used.</p>},
	keywords = {alkynols, cascade synthesis, chemoselectivity, diversity-oriented synthesis, Homogeneous catalysis},
	issn = {0947-6539},
	doi = {10.1002/chem.201405736},
	author = {Bansode, Avinash H. and Shaikh, Aslam C. and Kavthe, Rahul D. and Thorat, Shridhar and Gonnade, Rajesh G. and Patil, Nitin T.}
}
@article {42850,
	title = {Catalytic branching cascades in diversity oriented synthesis},
	journal = {ChemCatChem},
	volume = {9},
	year = {2017},
	month = {OCT},
	pages = { 30-40},
	type = {Article},
	abstract = {<p>Diversity oriented synthesis (DOS) aims to generate small molecules with great structural diversity in an efficient manner. Recent years have witnessed significant achievements in the field, which help to validate the usefulness of DOS as a tool for the discovery of novel, biologically interesting small molecules. Catalytic branching cascades have emerged as a promising strategy because of their potential to transform a common type of substrate into diverse and distinct molecular frameworks. The details of the concept are presented herein.</p>},
	doi = {10.1002/cctc.201600766},
	author = {Bansode, Avinash H. and Chimala, Prathyusha and Patil, Nitin T.}
}
@article {43359,
	title = {Catalytic enantioselective aza-piancatelli rearrangement},
	journal = {Synlett},
	volume = {28},
	year = {2017},
	month = {JUN},
	pages = {1096-1100},
	type = {Article},
	abstract = {The design and development of an enantioselective aza-Piancatelli rearrangement reaction are described. In the presence of a chiral phosphoric acid catalyst, furylcarbinols react with anilines to afford highly functionalized cyclopentenones with excellent diastereo-and enantioselectivities. The process was shown to be scalable, and up to 1 gram of starting material could be employed under mild reaction conditions.},
	doi = {10.1055/s-0036-1558952},
	author = {Gade, Amol B. and Patil, Nitin T.}
}
@article {43877,
	title = {Cross-coupling reactions of aryldiazonium salts with allylsilanes under merged gold/visible-light photoredox catalysis},
	journal = {Organic Letters},
	volume = {19},
	year = {2017},
	month = {JUN},
	pages = {3075-3078},
	type = {Article},
	abstract = {A method for the cross-coupling reactions of aryldiazonium salts with trialkylallylsilanes via merged gold/photoredox catalysis is described. The reaction is proposed to proceed through a photoredox-promoted generation of an electrophilic arylgold(III) intermediate that undergoes transmetalation with allyltrimethylsilane to form allylarenes.},
	doi = {10.1021/acs.orglett.7b01148},
	author = {Akram, Manjur O. and Mali, Pramod S. and Patil, Nitin T.}
}
@article {44374,
	title = {Catalytic enantioselective 1,3-alkyl shift in alkyl aryl ethers: efficient synthesis of optically active 3,3 {\textquoteright}-diaryloxindoles},
	journal = {Angewandte Chemie-International Edition},
	volume = {57},
	year = {2018},
	month = {MAY},
	pages = {5735-5739},
	abstract = {Reported is the first organocatalytic asymmetric 1,3-alkyl shift in alkyl aryl ethers for the synthesis of chiral 3,3{\textquoteright}-diaryloxindoles using a chiral Bronsted acid catalyst. Preliminary results showed that each enantiomer of the 3,3{\textquoteright}-diaryloxindole, and a racemic mixture, showed different antiproliferative activities against HeLa cell lines by using an MTT assay.},
	doi = {10.1002/anie.201801650},
	author = {Gade, Amol B. and Bagle, Pradip N. and Shinde, Popat S. and Bhardwaj, Vipin and Banerjee, Subhrashis and Chande, Ajit and Patil, Nitin T.}
}
