Jacob III et al., 1981 - Google Patents
Sulfur analogues of psychotomimetic agents. Monothio analogs of mescaline and isomescalineJacob III et al., 1981
View PDF- Document ID
- 8493902048653307875
- Author
- Jacob III P
- Shulgin A
- Publication year
- Publication venue
- Journal of Medicinal Chemistry
External Links
Snippet
Two monothio analogues of mescaline and threemonothio analogues of 2, 3, 4- trimethoxyphenethylamine (isomescaline) have been synthesized and characterized. Only the two mescaline analogues (3-and 4-thiomescaline) were found to be psychotomimetics in …
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 COC1=CC(CCN)=CC(OC)=C1OC 0 title abstract description 35
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/12—Systems containing only non-condensed rings with a six-membered ring
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