Substitution, Oxidation and Addition Reactions at C-7 of Activated Indoles

DOI: 10.1016/S0040-4020(01)89590-9

Source and publish data:

Tetrahedron p. 10497 - 10508 (1994)

Update date:2022-08-05

Topics:

Authors:

Black, David St.C.

Bowyer, Michael C.

Catalano, Maria M.

Ivory, Andrew J.

Keller, Paul A.

et al. et al.

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Article abstract of DOI:10.1016/S0040-4020(01)89590-9

4,6-Dimethoxy-2,3-diphenylindole (1) undergoes acylation, bromination, oxidative coupling and acidcatalysed addition to aldehydes at C-7 to produce a range of 7-substituted indoles (3-11), the indolo-isatin (6), the 7,7'-bi-indolyls (14), (16), (18), and

Full text of DOI:10.1016/S0040-4020(01)89590-9

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