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Tnfluoromethyl hypofluonte

With more electrophilic halogenated olefins, additions of tnfluoromethyl hypofluonte appear to go by radical processes [139] and give oligomeric products [140] or one-to-one adducts [141,142] (equation 4) depending on reaction conditions... [Pg.70]

Tnfluoromethyl hypofluonte will fluorinate Schiff bases, giving N,a,a-tn-fluoroatmnes and a-fluoroimines [144] and reacts with diazoketones to give adducts in modest yields [145] (equation 6) At-Substituted aziridines give nng opened products by 1,3 addition of fluonne on nitrogen and trifluoromethoxy on carbon [146] (equation 7)... [Pg.70]


See other pages where Tnfluoromethyl hypofluonte is mentioned: [Pg.26]    [Pg.70]    [Pg.26]    [Pg.70]   


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Addition of halogen fluonde tnfluoromethyl hypofluonte

Hypofluontes

Tnfluoromethylation

With tnfluoromethyl hypofluonte

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