Biomimetic Syntheses of Indole Alkaloids. 11. Syntheses of β-Carboline and Indoloazepine Intermediates

DOI: 10.1021/jo00207a001

Source and publish data:

Journal of Organic Chemistry p. 919 - 924 (1985)

Update date:2022-09-26

Topics:

Authors:

Kuehne, M. E.

Bohnert, J. C.

Bornmann, W. G.

Kirkemo, C. L.

Kuehne, S. E.

et al. et al.

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Article abstract of DOI:10.1021/jo00207a001

The preparation and rearrangement of α-carbomethoxy-α-(chloromethyl)tetrahydro-β-carbolines (9a,b) provided methyl 1,2,3,6-tetrahydroazepino<4,5-b>indole-5-carboxylates (10a,b) and derivatives, which serve as intermediates in a series of alkaloid synthese

Full text of DOI:10.1021/jo00207a001

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