Regiocontrolled Annellation Reactions Starting from Diethoxymethyl Protected Indole

Gmeiner P (2000)

Publication Type: Journal article

Publication year: 2000

Journal

Synthesis-Stuttgart Thieme Publishing / Georg Thieme Verlag

Publisher: Thieme Publishing / Georg Thieme Verlag

Pages Range: 1081-1083

DOI: 10.1055/s-2000-6329

Abstract

Directed metallation of the diethoxymethyl protected indole 4 followed by treatment with β-nitrostyrene leads to the 1,2- disubstituted indole 5. Using 5 as a central intermediate, the tricyclic annellation products of type 2 and 3 were accessed when the regiochemical outcome of the reactions could be controlled.

Authors with CRIS profile

Peter Gmeiner Lehrstuhl für Pharmazeutische Chemie

How to cite

APA:

Gmeiner, P. (2000). Regiocontrolled Annellation Reactions Starting from Diethoxymethyl Protected Indole. Synthesis-Stuttgart, 1081-1083. https://doi.org/10.1055/s-2000-6329

MLA:

Gmeiner, Peter. "Regiocontrolled Annellation Reactions Starting from Diethoxymethyl Protected Indole." Synthesis-Stuttgart (2000): 1081-1083.

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