Preparation and Bromination of a 3a,6-Dihydroindole

DOI: 10.1021/jo01311a005

Source and publish data:

Journal of Organic Chemistry p. 4582 - 4584 (1980)

Update date:2022-08-05

Topics:

Authors:

Noland, Wayland E.

Kim, Keun Jae

Lee, Chang Kiu

Bae, Sun Kun

Hahn, Chi Sun

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Article abstract of DOI:10.1021/jo01311a005

A 3a,6-dihydroindole was prepared by the Diels-Alder addition of dimethyl acetylenedicarboxylate to dimethyl maleate. Subsequent reaction with bromine gave a 2,3-dibromoindoline which is different from that obtained from the corresponding 3a,7a-dihydroindole.

Full text of DOI:10.1021/jo01311a005

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