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0-Phen ethylamines

Bell, S.E., Bums, D.T., Dennis, A.C., and Speers, J.S., Rapid analysis of ecstasy and related phen-ethylamines in seized tablets by Raman spectroscopy, Analyst 125(3), 541-544, 2000. [Pg.135]

As an extension of the above-mentioned method, a successful rearrangement starting from silyl enol ethers as an electron-rich iV-allyl moiety has been published. Allylamide 88 was synthesized in two steps starting from (-i-)-phen-ethylamine and acrolein via a condensation-acylation sequence. The auxiliary-... [Pg.169]

EXTENSIONS AND COMMENTARY Here is the first example, ever, of a phen-ethylamine that is of about the same potency as therelated three-carbon amphetamine. At first approximation, one is hard put to distinguish, from the recorded notes, any major differences either in potency, in duration, or in the nature of activity, between 2C-G and GANESHA itself. [Pg.273]

Also synthesized are 2-6-dichloral-TMPEA (trimethoxy- j8 -phen-ethylamine) and 2-chloraI-TMPEA—these are the 2,6-dichloral and 2-chloral analogues of mescaline—and 4-thiomescaline, a compound in which a sulfur atom replaces oxygen in the 4-position. The last has been found to affect the central nervous system. In the Journal of Psychedelic Drugs forjanuary-june... [Pg.226]

Both of these compounds possess a /3-phen-ethylamine framework, a common structural theme that occurs in many related CNS stimulants. In general, these compounds have similar mechanisms of action. [Pg.169]

The majority of appetite-suppressant drugs are congeners of 2-phenethylamine ()3-phen-ethylamine, 37), a compound with close struc-... [Pg.855]

The basic skeleton of the adrenaline molecule is that of a /9-phen-ethylamine. In 1910, when Barger and coworkers made their first studies, only three naturally occurring compounds of this type were... [Pg.313]

According to Barger and Dale, the relative effects of some 3-phen-ethylamines on blood pressure in decerebrated cats (isoamylamine = 1) are ... [Pg.330]

Thus, they are kind of a dead end, at least as far as the 2C-X series is considered. The heaviest, iodine, was explored as the phen-ethylamine, as 2C-I, and as the amphetamine as DOI. These are the most potent. The next lighter is bromine, where the phenethylamine is 2C-B and the amphetamine is DOB. These two are a bit less potent, and are by far the most broadly explored of all the halides. Here, in the above recipe, we have the chlorine counterpart,... [Pg.694]

A few species of the Fabaceae family (Table 4) contain the tetrahydroisoquinoline alkaloids salsoline and salsolidine that are also found in the Cactaceae and the Cheno-podiaceae. It is interesting to note that the Alhagi and Desmodium species investigated by Ghosal et al. (1973a, b, 1974) also contain a variety of substituted -phen-ethylamines. The Fabaceae family belongs to the order of Fabales, that is deeply... [Pg.55]


See other pages where 0-Phen ethylamines is mentioned: [Pg.60]    [Pg.266]    [Pg.138]    [Pg.395]    [Pg.234]    [Pg.246]    [Pg.98]    [Pg.54]    [Pg.237]    [Pg.101]    [Pg.103]    [Pg.1714]    [Pg.286]    [Pg.177]    [Pg.196]    [Pg.61]    [Pg.1637]    [Pg.2507]    [Pg.95]    [Pg.61]    [Pg.484]   
See also in sourсe #XX -- [ Pg.47 , Pg.51 , Pg.52 , Pg.54 ]




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Ethylamines

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