@article { ISI:000340526400001,
	title = {Stable silanone with a three-coordinate silicon atom: a century-long wait is over},
	journal = {Angewandte Chemie-International Edition},
	volume = {53},
	number = {34},
	year = {2014},
	month = {AUG},
	pages = {8820-8822},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	keywords = {cations, germanones, Ketones, silanones, transition metals},
	issn = {1433-7851},
	doi = {10.1002/anie.201404793},
	author = {Sen, Sakya S.}
}
@article { ISI:000357617800013,
	title = {Reduced graphene oxide composite with oxidizable manganese/cobalt mixed oxide for p-cresol oxidation by using molecular oxygen},
	journal = {ChemPlusChem},
	volume = {80},
	number = {7},
	year = {2015},
	month = {JUL},
	pages = {1164-1169},
	publisher = {WILEY-V C H VERLAG GMBH},
	type = {Article},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>A composite of graphene oxide (GO) with mixed oxide (MnCo) was prepared by using a solvothermal method. During the synthesis, both the reduction of GO and growth of metal oxides took place simultaneously. The as-prepared composite material was highly selective for the liquid-phase oxidation of p-cresol to form p-hydroxybenzaldehyde in 71\% yield within 1h. The composite material was characterised by SEM, X-ray photoelectron spectroscopy, high-resolution TEM and cyclic voltammetry (CV). A CV study revealed that the increase in the redox potential of the mixed oxide after being supported on GO, led to its higher activity of the catalyst for the oxidation reaction. The stability of the catalyst under the reaction conditions was studied by its successful reuse in three cycles.</p>},
	keywords = {cyclic voltammetry, graphene, Oxidation, supported catalysts, transition metals},
	issn = {2192-6506},
	doi = {10.1002/cplu.201500053},
	author = {Jha, Ajay and Patil, Sagar H. and Solanki, Bhanu P. and Ribeiro, Ana P. C. and Castro, Carlos A. N. and Patil, Kashinath R. and Coronas, Alberto and Rode, Chandrashekhar V.}
}
@article {47036,
	title = {Unactivated alkyl halides in transition-metal-catalyzed C-H bond alkylation},
	journal = {ACS Catalysis},
	volume = {11},
	year = {2021},
	month = {MAR },
	pages = {3268-3292},
	type = {Review},
	abstract = {<p>Alkylation represents an important organic transformation in molecular science to develop privileged alkylated arenes and heteroarenes. Especially, the direct C-H bond alkylation using unactivated alkyl halides is a straightforward and attractive approach from both the step-economy and chemoselectivity perspectives. Substantial progress has been made in the direct alkylation using primary, secondary, and tertiary alkyl halides along with the methylation and fluoroalkylation. This Review broadly summarizes the transition-metal-catalyzed alkylations of C-H bonds on various arenes and heteroarenes with unactivated alkyl halides until October 2020. On the basis of the substrates utilized for alkylation, the Review is divided into two major sections: alkylation of arenes and alkylation of heteroarenes.</p>
},
	keywords = {(hetero)arenes, Alkylation, C-H activation, transition metals, unactivated alkyl halides},
	issn = {2155-5435},
	doi = {10.1021/acscatal.0c05580},
	author = {Ankade, Shidheshwar B. and Shabade, Anand B. and Soni, Vineeta and Punji, Benudhar}
}
