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Carbinolamine Carbocations

Carbinolamines are formed by nucleophilic addition of an amine to a carbonyl group and are intermediates in the for mation of imines and enamines Carbocation (Section 4 8) Positive ion in which the charge re sides on carbon An example is tert butyl cation (CH3)3C Carbocations are unstable species that though they cannot normally be isolated are believed to be intermediates in certain reactions... [Pg.1278]

Step 4 The oxygen-protonated carbinolamine loses water to give a nitrogen-stabilized carbocation. [Pg.732]

Carbenes and carbenoids, 565—566, 571—572 Carbenium ions, 140. See also Carbocations Carbinolamine intermediates, 672—673, 674 Carbobenzoxy. See Benzyloxycarbonyl Carbocations... [Pg.1219]


See other pages where Carbinolamine Carbocations is mentioned: [Pg.1289]    [Pg.629]    [Pg.732]    [Pg.747]    [Pg.1396]   
See also in sourсe #XX -- [ Pg.52 , Pg.87 ]




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Carbinolamine

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