@article {43568,
	title = {Expeditious and solvent-free nickel-catalyzed C-H arylation of arenes and indoles},
	journal = {ChemSusChem},
	volume = {10},
	year = {2017},
	month = {APR},
	pages = {2242-2248},
	type = {Article},
	abstract = {An efficient solvent-free nickel-catalyzed method for C-H bond arylation of arenes and indoles has been developed, which proceeds expeditiously through chelation assistance. The reaction is highly selective for mono-arylation and tolerates sensitive and structurally diverse functionalities, such as halides, ethers, amines, indole, pyrrole and carbazole. This reaction represents the first example of a nickel-catalyzed C-H arylation by monochelate assistance and symbolizes a rare precedent in solvent-free C-H arylation. Mechanistic investigations by various controlled reactions, kinetic studies, and deuterium labeling experiments suggest that the arylation follows a single electron transfer (SET) pathway involving the turnover-limiting C-H nickelation process.},
	doi = {10.1002/cssc.201700321},
	author = {Jagtap, Rahul A. and Soni, Vineeta and Punji, Benudhar}
}
@article {46673,
	title = {Expeditious and solvent-free nickel-catalyzed c-h arylation of arenes and indoles (vol 10, pg 2242, 2017)},
	journal = {ChemSusChem},
	volume = {13},
	year = {2020},
	month = {NOV },
	pages = {5771},
	type = {Correction},
	keywords = {Arylation, C-H activation, heterocycles, Homogeneous catalysis, Nickel},
	issn = {1864-5631},
	doi = {10.1002/cssc.202002313, Early Access Date = OCT 2020},
	author = {Jagtap, Rahul A. and Soni, Vineeta and Punji, Benudhar}
}
