Further studies on oxygenated tryptamines with LSD-like activity incorporating a chiral pyrrolidine moiety into the side chain
The enantiomers of 3-(N-methylpyrrolidin-2-ylmethyl)-5-methoxyindole, 1, and 3-(N-methylpyrrolidin-2-ylmethyl)-4-hydoxyindole, 3, were prepared using an asymmetric synthesis that employed (+)- or (-)-proline. A new approach was developed that had certain
Gerasimov, Madina,Marona-Lewicka, Danuta,Kurrasch-Orbaugh, Deborah M.,Qandil, Amjad M.,Nichols, David E.
p. 4257 - 4263
(2007/10/03)
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