@article {46347,
	title = {Acidic handle assemble heterogeneous carbocatalyst for facile aliphatic nucleophilic fluorination},
	journal = {ChemistrySelect},
	volume = {4},
	year = {2019},
	month = {SEP },
	pages = {10960-10964},
	type = {Article},
	abstract = {<p>Acidic handle (-SO3H) assemble carbonaceous catalyst synthesized from glucose acts as a modulator for the nucleophilic fluorination reaction. The heterogeneous catalyst works with various alkyl sulfonate, halide and metal fluoride (MF), to offer a high yield of fluorinated products up to 93\%. This carbonaceous catalyst is recyclable for more than five times, with no major loss of activity.</p>
},
	keywords = {fluorination, heterogeneous catalysis},
	issn = {2365-6549},
	doi = {10.1002/slct.201902771},
	author = {Said, Madhukar S. and Pandole, Satish and Suryavanshi, Amol and Kumar, Pradeep and Gajbhiye, Jayan M.}
}
@article {46332,
	title = {Regioselective one-pot synthesis of 3-fluoro-imidazo[1,2-a]pyridines from styrene},
	journal = {Asian Journal of Organic Chemistry},
	year = {2019},
	month = {OCT},
	type = {Article; Early Access},
	abstract = {<p>A one-pot synthesis of C-3 fluorinated imidazopyridines (F-IMPY) is reported under the additive-free conditions from commercially available styrene and 1-fluoropyridinium tetrafluoroborate as a fluorine source. The substrate styrene undergoes keto-bromination/condensation/fluorination transformation in three sequential steps to furnish F-IMPY. This one-pot synthesis method exhibits broad substrate scope and good functional group tolerance with a good yield (up to 82\%).</p>
},
	keywords = {fluorination, imidazopyridines (F-IMPY), One-pot synthesis},
	issn = {2193-5807},
	doi = {10.1002/ajoc.201900521},
	author = {Said, Madhukar S. and Mishra, Ankita and Pandole, Satish and Nayak, Rashmi A. and Kumar, Pradeep and Gajbhiye, Jayant M.}
}
