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Biosynthesis of mescaline

K. L. Khanna, H. Rosenberg, A.g. Paul

Journal of the Chemical Society D Chemical Communications January 1, 1969 DOI: 10.1039/c29690000315 (opens in new tab) via OpenAlex

Summary

AI-generated from the abstract

A proposed biosynthetic pathway suggests that mescaline is produced from 3,4-dihydroxy phenethylamine through m-O-methylation, a chemical modification that adds methyl groups to specific oxygen atoms. This outlines a potential natural route for the formation of the psychoactive compound.

Study at a glance

Characteristics Theoretical or philosophical paper Peer reviewed
Topics Mescaline
Keywords Phenethylamine Biosynthesis Methylation Stereochemistry
Citations 7
Key finding Proposes that mescaline biosynthesis occurs from 3,4-dihydroxy phenethylamine via m-O-methylation.

Abstract

A pathway of biosynthesis of mescaline from 3,4-dihydroxy phenethylamine via m-O-methylation is proposed.

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