Investigation of the Bischler Indole Synthesis from 3,5-Dimethoxyaniline

DOI: 10.1071/CH9800343

Source and publish data:

Australian Journal of Chemistry p. 343 - 350 (1980)

Update date:2022-08-05

Topics:

Authors:

Black, David St.C.

Gatehouse, Bryan M.K.C.

Theobald, Francois

Wong, Laurence C.H.

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Article abstract of DOI:10.1071/CH9800343

Cyclization of the amino ketones (3a,b) derived from 3,5-dimethoxyaniline, and phenacyl bromide and 4-bromophenacyl bromide respectively, afforded 2-arylindoles (8a,b) in preference to 3-arylindoles (7).The 3-(4'bromophenyl)indole (7b) was also isolated i

Full text of DOI:10.1071/CH9800343

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