@article {46099,
	title = {Nickel(ii)-catalyzed direct olefination of benzyl alcohols with sulfones with the liberation of H-2},
	journal = {Chemical Communications},
	volume = {55},
	year = {2019},
	month = {MAY },
	pages = {6130-6133},
	type = {Article},
	abstract = {<p>A nickel(II)-catalyzed direct olefination of benzyl alcohols with sulfones to access various terminal and internal olefins with the liberation of hydrogen gas is reported.</p>
},
	issn = {1359-7345},
	doi = {10.1039/c9cc02603g},
	author = {Landge, Vinod G. and Yadav, Vinita and Subaramanian, Murugan and Dangarh, Pragya and Balaraman, Ekambaram}
}
@article {48343,
	title = {Nickel-catalyzed direct synthesis of N-substituted indoles from amino alcohols and alcohols},
	journal = {Organic Letters},
	volume = {24},
	year = {2022},
	month = {DEC},
	pages = {9054-9059},
	type = {Article},
	abstract = {<p>
	A one-pot cascade approach for the synthesis of N substituted indoles from amino alcohols and alcohols under additive and base-free conditions with the liberation of water as the only stoichiometric byproduct is reported. The commercially available bench-stable Ni(OTf)2 salt in combination with 1,2-bis(dicyclohexylphosphino)ethane (dcype) is very effective for this unprecedented catalytic transformation. A broad range of substrates including aromatic and aliphatic primary alcohols, cyclic and acyclic secondary alcohols, and various substituted 2-aminophenyl ethyl alcohols are employed in the reaction conditions to provide a diverse range of N-alkylated indoles. Mechanistic studies revealed that the reaction proceeds through tandem N-alkylation via hydrogen autotransfer followed by the cyclization of N-alkylated alcohol intermediate.</p>
},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.2c03617},
	author = {Yadav, Vinita and Jagtap, Sayali G. and Balaraman, Ekambaram and Mhaske, Santosh B.}
}
