Limpet_Chicken
Bluelighter
- Joined
- Oct 13, 2005
- Messages
- 6,323
DOI 10.1002/dta.413 Fluorinated psychedelic phenethylamines
Interesting reading, although it didn't tell me what I wish to know.
What is known of 4-difluoromethoxy,5-methoxyphenethylamines, amphetamines, phentermines, cathinones, cathinthiones or cathinone selenoketone homologs which also bear a 3-substituent of electron-withdrawing/strongly electronegative substituents. In particular halogens (in this case, a bromo group, although halex reactions like the finkelstein should afford more scope if there should prove reason to do so)
And how about the thioketone and selenoketone homologs of the corresponding cathinone. Lawesson's or Woolin's should do the trick. Allthough question is, would they be possessed of a terrible stench?
because I sure as hell wouldn't want to be the poor bastard who has to face up to giving birth to something that behaved like thioacetone. And as we generally know, where sulfur stinks, selenium stinks worse.
Interesting reading, although it didn't tell me what I wish to know.
What is known of 4-difluoromethoxy,5-methoxyphenethylamines, amphetamines, phentermines, cathinones, cathinthiones or cathinone selenoketone homologs which also bear a 3-substituent of electron-withdrawing/strongly electronegative substituents. In particular halogens (in this case, a bromo group, although halex reactions like the finkelstein should afford more scope if there should prove reason to do so)
And how about the thioketone and selenoketone homologs of the corresponding cathinone. Lawesson's or Woolin's should do the trick. Allthough question is, would they be possessed of a terrible stench?
because I sure as hell wouldn't want to be the poor bastard who has to face up to giving birth to something that behaved like thioacetone. And as we generally know, where sulfur stinks, selenium stinks worse.