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Indole-2,3-quinodimethanes, intermolecular cycloaddition reactions

Aminomethylindoles are particularly important synthetic intermediates. 3-Dimethyl-aminomethylindole (gramine) (153) and especially its quaternary salts readily undergo displacement reactions with nucleophiles (Scheme 60). Indole-2,3-quinodimethanes, generated from 2-methylgramine as shown in Scheme 61, undergo intermolecular cycloaddition reactions with dienophiles to yield carbazole derivatives (82T2745). [Pg.71]

Indole-2,3-quinodimethanes, generated from 2-methylgramine, undergo intermolecular cycloaddition reactions with dienophiles similar to that of (325) (82T2745). [Pg.350]


See other pages where Indole-2,3-quinodimethanes, intermolecular cycloaddition reactions is mentioned: [Pg.91]    [Pg.462]   
See also in sourсe #XX -- [ Pg.454 ]




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Cycloaddition reactions intermolecular

Indole cycloaddition

Indole reactions

Indole-2,3-quinodimethane

Indole-2,3-quinodimethanes

Indole-2,3-quinodimethanes, cycloaddition reactions

Indoles 2 + 2 + 2] cycloaddition reactions

Indoles 2,3-quinodimethanes

Indoles reactions

Indoles, cycloaddition

Quinodimethane

Quinodimethanes

Quinodimethanes, cycloaddition

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