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• W2338572034 endingPage "1855" @default.
• W2338572034 startingPage "1852" @default.
• W2338572034 abstract "The superior nucleofuge character of chlorine over fluorine was taken advantage of in the selective SN2' substitution reaction of gem-chlorofluoropropenes, allowing for the clean formation of β-substituted monofluoroalkenes under metal-free conditions. Numerous N-, S-, O-, and C-nucleophiles behaved nicely in this system. Further synthetic transformations of selected monofluoroalkenes were also accomplished." @default.
• W2338572034 created "2016-06-24" @default.
• W2338572034 creator A5083701547 @default.
• W2338572034 creator A5089379813 @default.
• W2338572034 creator A5091327960 @default.
• W2338572034 date "2016-04-04" @default.
• W2338572034 modified "2023-10-06" @default.
• W2338572034 title "Exploiting a Difference in Leaving Group Ability: An Approach to β-Substituted Monofluoroalkenes Using <i>gem</i>-Chlorofluoropropenes" @default.
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• W2338572034 doi "https://doi.org/10.1021/acs.orglett.6b00590" @default.
• W2338572034 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27043817" @default.
• W2338572034 hasPublicationYear "2016" @default.
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