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• W3189742667 endingPage "13204" @default.
• W3189742667 startingPage "13195" @default.
• W3189742667 abstract "Addition of halomethyl radicals to form bioactive molecules has recently become an efficient strategy. The reaction has a bottleneck, however, which is the effective and selective generation of the proper halomethyl •CHnX3-n radical by combining CHnX4-n with a carbon radical. Understanding the reactivity and selectivity of carbon radicals in the hydrogen atom transfer (HAT) and halogen atom transfer (XAT) reactions of CHnX4-n is key to the development of such an attractive method. With the help of the emerging data-driven strategy, DFT calculations were used to explore various correlations. For selectivity, the relative energy barriers between HAT and XAT reactions (ΔG⧧H - ΔG⧧X) correlate reasonably well with the three parameters ΔGH, ΔGX, and IP, and the correlation studies reveal that the calculated IPinver and the experimental ΔBDE can be used to conveniently predict the selectivity. Predicted selectivities are consistent with experimental determinations. This work not only provides a possibility for selecting carbon radicals with the known or easily obtained physicochemical data but also demonstrates that the informatic workflow such as generating data and identifying correlations has potential applications in mining reaction rules." @default.
• W3189742667 created "2021-08-16" @default.
• W3189742667 creator A5004078791 @default.
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• W3189742667 date "2021-08-10" @default.
• W3189742667 modified "2023-10-15" @default.
• W3189742667 title "Precise Introduction of the −CH_<i>n</i>X_3–<i>n</i> (X = F, Cl, Br, I) Moiety to Target Molecules by a Radical Strategy: A Theoretical and Experimental Study" @default.
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• W3189742667 doi "https://doi.org/10.1021/jacs.1c05208" @default.
• W3189742667 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34374531" @default.
• W3189742667 hasPublicationYear "2021" @default.
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