Literature DB >> 22374819

Fluorine in psychedelic phenethylamines.

Daniel Trachsel1.   

Abstract

The so-called psychedelic phenethylamines represent a class of drugs with a large range of psychoactive properties in humans, ranging from naturally occurring mescaline to amphetamine analogues and homologues. The interest in many of these compounds, occasionally referred to as designer-drugs, is widely dispersed across popular culture and political and scientific communities. In recent decades, fluorine has become a powerful and important tool in medicinal chemistry. In addition, fluorine-containing compounds and medicines can be found in numerous commercially successful pharmaceuticals that have gained a market share of some 5-15%. One might anticipate this trend to increase in the future. As far as fluorinated phenethylamines are concerned, much less is known about their chemistry and pharmacology. This paper provides an overview regarding the biological properties of over 60 fluorinated phenethylamines and discusses both historical and recent chemistry-related developments. It was shown that the introduction of fluorine into the phenethylamine nucleus can impact greatly on psychoactivity of these compounds, ranging from marked loss to enhancement and prolongation of effects. For example, in contrast to the psychoactive escaline (70), it was observed that its fluoroescaline (76) counterpart was almost devoid of psychoactive effects. Difluoroescaline (77), on the other hand, retained, and trifluoroescaline (78) showed increased human potency of escaline (70). Difluoromescaline (72) and trifluoromescaline (73) increasingly surpassed human potency and duration of mescaline (22) effects.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22374819     DOI: 10.1002/dta.413

Source DB:  PubMed          Journal:  Drug Test Anal        ISSN: 1942-7603            Impact factor:   3.345


  6 in total

1.  Catalytic Diastereo- and Enantioselective Fluoroamination of Alkenes.

Authors:  Katrina M Mennie; Steven M Banik; Elaine C Reichert; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2018-03-29       Impact factor: 15.419

2.  Ethanol: Unlocking an Abundant Renewable C2 -Feedstock for Catalytic Enantioselective C-C Coupling.

Authors:  Cole C Meyer; Nicholas P Stafford; Melinda J Cheng; Michael J Krische
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-30       Impact factor: 15.336

3.  Diastereo- and Enantioselective Ruthenium-Catalyzed C-C Coupling of 1-Arylpropynes and Alcohols: Alkynes as Chiral Allylmetal Precursors in Carbonyl anti-(α-Aryl)allylation.

Authors:  Ming Xiang; Ankan Ghosh; Michael J Krische
Journal:  J Am Chem Soc       Date:  2021-02-08       Impact factor: 15.419

4.  Receptor Interaction Profiles of 4-Alkoxy-Substituted 2,5-Dimethoxyphenethylamines and Related Amphetamines.

Authors:  Karolina E Kolaczynska; Dino Luethi; Daniel Trachsel; Marius C Hoener; Matthias E Liechti
Journal:  Front Pharmacol       Date:  2019-11-28       Impact factor: 5.810

5.  Receptor Interaction Profiles of 4-Alkoxy-3,5-Dimethoxy-Phenethylamines (Mescaline Derivatives) and Related Amphetamines.

Authors:  Karolina E Kolaczynska; Dino Luethi; Daniel Trachsel; Marius C Hoener; Matthias E Liechti
Journal:  Front Pharmacol       Date:  2022-02-09       Impact factor: 5.810

6.  Catalytic Enantioselective Synthesis of Heterocyclic Vicinal Fluoroamines by Using Asymmetric Protonation: Method Development and Mechanistic Study.

Authors:  Matthew W Ashford; Chao Xu; John J Molloy; Cameron Carpenter-Warren; Alexandra M Z Slawin; Andrew G Leach; Allan J B Watson
Journal:  Chemistry       Date:  2020-08-18       Impact factor: 5.236

  6 in total

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