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Indole Grignard reagents with aldehydes

This new indole ring synthesis should find utility for the preparation of 2-aryUndoles with electron-withdrawing substituents in the indole ring. Furthermore, as we see in equations 1-3, the bromine atom is impervious to attack by the Grignard reagent. The starting ortfto-nitrostilbenes were prepared in the standard fashion from the appropriate ortho-nitrotoluene and aryl aldehyde with piperidine as base. [Pg.299]


See other pages where Indole Grignard reagents with aldehydes is mentioned: [Pg.819]    [Pg.88]    [Pg.81]    [Pg.819]    [Pg.36]    [Pg.452]    [Pg.452]    [Pg.819]    [Pg.44]    [Pg.88]    [Pg.819]    [Pg.106]    [Pg.171]   
See also in sourсe #XX -- [ Pg.10 , Pg.86 ]




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Aldehydes Grignard reagents

Aldehydes reagents

Aldehydes with Grignard reagents

Indole Grignard reagents

Indoles => aldehydes

Reagents indole

With Grignard Reagents

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