Psilocin analogs. 1. Synthesis of 3‐[2‐(dialkylamino)ethyl] ‐and 3‐[2‐(cycloalkylamino)ethyl] indol‐4‐ols
Document Type
Article
Publication Date
1-1-1977
Department
Department of Chemistry; Department of Chemical Engineering
Abstract
The synthesis of four dialkyl and three eyeloalkyl analogs of psilocin (4, R ‐ CH3), a hallucinogenic principle found in certain fungi, is described. The synthetic route involves four transformations starting with 6,7‐dihydroindol‐4(5H)one: (1).
Publication Title
Journal of Heterocyclic Chemistry
Recommended Citation
Repke, D.,
Ferguson, W.,
&
Bates, D.
(1977).
Psilocin analogs. 1. Synthesis of 3‐[2‐(dialkylamino)ethyl] ‐and 3‐[2‐(cycloalkylamino)ethyl] indol‐4‐ols.
Journal of Heterocyclic Chemistry,
14(1), 71-74.
http://doi.org/10.1002/jhet.5570140113
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/3739
Publisher's Statement
Copyright © 1977 Journal of Heterocyclic Chemistry. Publisher’s version of record: https://doi.org/10.1002/jhet.5570140113