@article { ISI:000253334800010,
	title = {Dimethyl sulfoxide pivaloyl chloride: a new reagent for oxidation of alcohols to carbonyls},
	journal = {Synthetic Communications},
	volume = {38},
	number = {5},
	year = {2008},
	month = {FEB},
	pages = {746-753},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>An efficient procedure for conversion of alcohols to the corresponding carbonyl compounds, an alternative to the classical Swern oxidation, is described. Pivaloyl chloride is employed as a mild and inexpensive electrophile. A possible reaction mechanism is proposed.</p>},
	keywords = {Alcohols, carbonyls, DMSO, pivaloyl chloride, Swern oxidation},
	issn = {0039-7911},
	doi = {10.1080/00397910701820343},
	author = {Dubey, Abhishek and Kandula, Subba Rao V. and Kumar, Pradeep}
}
@article {48930,
	title = {Electron-deficient fluoroarene-mediated synthesis of trifluoromethyl ketones from carboxylic acids},
	journal = {Organic Letters },
	year = {2023},
	month = { FEB },
	type = {Article; Early Access},
	abstract = {<p>Fluoroarene-mediated trifluoromethylation of carboxylic acids for the synthesis of trifluoromethyl ketones is disclosed. The fluoroarene activates the acid group and generates the fluoride source in situ for the trifluoromethylation reaction. The present protocol is safe and metal-free, operates under mild reaction conditions, and does not require any external additives to generate trifluoromethyl anion. The current transformation provides good functional group tolerance and also delivers 92\% and 88\% yields of trifluoromethyl ketones in batch and continuous flow, respectively.</p>
},
	keywords = {Alcohols, amines, indoles, Oxidation, Trifluoroacetylation},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.2c04318},
	author = {Said, Madhukar S. and Khonde, Nilesh S. and Kumar, Pradeep and Gajbhiye, Jayant M.}
}
