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1

Assessing the atmospheric fate of trifluoroacetaldehyde (CF3CHO) and its potential as a new source of fluoroform (HFC-23) using the AtChem2 box model. Maria Paula Pérez-Peña, Jenny A. Fisher, Christopher Hansen, Scott H. Kable , Environ. Sci.: Atmos. , 2023 , 3 , 1767

Fluoroalkylation reactions in aqueous media: a review. Hai-Xia Song, Qiu-Yan Han, Cheng-Long Zhao, Cheng-Pan Zhang , Green Chem. , 2018 , 20 , 1662

Stereodivergent trifluoromethylation of N-sulfinylimines by fluoroform with either organic-superbase or organometallic-base. Nagender Punna, Takuya Saito, Mikhail Kosobokov, Etsuko Tokunaga, Yuji Sumii, Norio Shibata , Chem. Commun. , 2018 , 54 , 4294

Continuous flow strategies for using fluorinated greenhouse gases in fluoroalkylations. Wai Chung Fu, Preston M. MacQueen, Timothy F. Jamison , Chem. Soc. Rev. , 2021 , 50 , 7378

A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform. Hiroyuki Kawai, Zhe Yuan, Etsuko Tokunaga, Norio Shibata , Org. Biomol. Chem. , 2013 , 11 , 1446

Repurposing of F-gases: challenges and opportunities in fluorine chemistry. Daniel J. Sheldon, Mark R. Crimmin , Chem. Soc. Rev. , 2022 , 51 , 4977

Syntheses of [¹¹C]2- and [¹¹C]3-trifluoromethyl-4-aminopyridine: potential PET radioligands for demyelinating diseases. Karla M. Ramos-Torres, Yu-Peng Zhou, Bo Yeun Yang, Nicolas J. Guehl, Moon Sung-Hyun, Sanjay Telu, Marc D. Normandin, Victor W. Pike, Pedro Brugarolas , RSC Med. Chem. , 2020 , 11 , 1161

Domino cyclization/trifluoromethylation of 2-alkynylanilines using fluoroform-derived CuCF3: synthesis of 3-(trifluoromethyl)indoles. Yibin Ye, Kelvin Pak Shing Cheung, Lisi He, Gavin Chit Tsui , Org. Chem. Front. , 2018 , 5 , 1511

Copper(i)-free syntheses of [¹¹C/¹⁸F]trifluoromethyl ketones from alkyl or aryl esters and [¹¹C/¹⁸F]fluoroform. Susovan Jana, Sanjay Telu, Jimmy E. Jakobsson, Bo Yeun Yang, Victor W. Pike , Chem. Commun. , 2024 , 60 , 4589

Perfluoroalkyl derivatives of sulphur. Part II. Trifluoromethane-sulphonic, -sulphinic, and -sulphenic acid and the infrared spectra of compounds containing–SO2– and > S:O groups. R. N. Haszeldine, J. M. Kidd , J. Chem. Soc. , 1955 , 2901