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Diels-Alder reactions of nitroso compounds

Allyl amines can also be formed in an oxidative environment. Nicholas et al. have shown that instead of phenyl hydroxylamine as the nitrogen donor, it is possible using f-BuOOH as the terminal oxidant and the molybdenum catalyst described above [65]. The procedure is analogues to the in situ hetero-Diels-Alder reaction of nitroso compounds developed earlier by others [66]. [Pg.33]

See other pages where Diels-Alder reactions of nitroso compounds is mentioned: [Pg.269]    [Pg.270]   
See also in sourсe #XX -- [ Pg.514 , Pg.515 , Pg.516 , Pg.517 , Pg.518 , Pg.519 , Pg.520 , Pg.521 , Pg.522 , Pg.523 , Pg.524 , Pg.525 ]

See also in sourсe #XX -- [ Pg.514 , Pg.515 , Pg.516 , Pg.517 , Pg.518 , Pg.519 , Pg.520 , Pg.521 , Pg.522 , Pg.523 , Pg.524 , Pg.525 ]

See also in sourсe #XX -- [ Pg.514 , Pg.515 , Pg.516 , Pg.517 , Pg.518 , Pg.519 , Pg.520 , Pg.521 , Pg.522 , Pg.523 , Pg.524 , Pg.525 ]



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Diels-Alder reactions compounds

Nitroso compounds

Nitroso compounds Diels-Alder reactions

Nitroso compounds reaction

Of Diels-Alder reactions

Reactions of Nitroso Compounds

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