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Aromatic compounds nitrene additions

Trifluoroethanol has been shown to promote the addition of nitrenes, generated by the reaction of nitroso-compounds with phosphites, to aromatic hydrocarbons, e.g. (57), (58), and (59) are formed from the reaction... [Pg.243]

More importantly, this silver system catalyzes the intermolecular amination of hydrocarbons, as shown in Table 6.3. In addition to animating weaker benzylic C-H bonds, stronger aliphatic C-H bonds such as those in cyclohexane were also reactive. Although yields with more inert hydrocarbons were modest with the bathophenan-throline system, the discovery of the first silver-catalyzed intermolecular amination opens opportunities for further developments. This reaction favored tertiary cyclic sp3 C-H bonds over secondary cyclic sp3 C-H bonds, and showed limited success with simple linear alkanes. No conversion was observed with any aromatic C-H bonds. The compound NsNH2 was tested as the nitrene precursor with different oxidants. The use of PhI(OAc)2 as oxidant gave the expected amination product with a lower yield, while persulfate and peroxides showed no reactivity. [Pg.175]


See other pages where Aromatic compounds nitrene additions is mentioned: [Pg.5]    [Pg.114]    [Pg.88]    [Pg.96]    [Pg.692]    [Pg.7]    [Pg.395]    [Pg.56]    [Pg.48]    [Pg.51]   
See also in sourсe #XX -- [ Pg.338 ]




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