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3- indole, reaction with methoxybutenone

Interestingly, in the reaction of 2-methylindole with methoxybutenone, it is the indole -position, rather than the NH function, that is the reaction site to form 2-methyl-3-acetoxyvinylindole (251), the subsequent intramolecular cyclization of which leads to 2-methoxycarbazole 252 (62TL589). [Pg.220]


See other pages where 3- indole, reaction with methoxybutenone is mentioned: [Pg.217]    [Pg.218]   
See also in sourсe #XX -- [ Pg.82 , Pg.217 ]

See also in sourсe #XX -- [ Pg.82 , Pg.217 ]

See also in sourсe #XX -- [ Pg.82 , Pg.217 ]

See also in sourсe #XX -- [ Pg.82 , Pg.217 ]




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Methoxybutenones, reaction with

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