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Efficient one-pot synthesis of tryptamines and tryptamine homologues by amination of chloroalkynes
Tetrahedron Letters, 2004A new method was developed for the one-pot synthesis of substituted 3-(2-aminoethyl)- and 3-(3-aminopropyl)indoles from commercially available aryl hydrazines and chloroalkylalkynes. Various tryptamine derivatives were prepared directly in good yield with excellent regioselectivity.
Vivek Khedkar +3 more
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Journal of the Chemical Society, Perkin Transactions 1, 1979
2-Amino-1-o-bromophenylethanols (4) give indoles (5) when heated to 140–170 °C in a solution of ammonia in methanol. The reaction is suitable for the synthesis of a wide variety of 1-, 3-, 5-, and 6-substituted indoles and, because the starting materials are easy to make, it is particularly suitable for the synthesis of N(b)-di-substituted tryptamines (
Ian Fleming, Michael Woolias
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2-Amino-1-o-bromophenylethanols (4) give indoles (5) when heated to 140–170 °C in a solution of ammonia in methanol. The reaction is suitable for the synthesis of a wide variety of 1-, 3-, 5-, and 6-substituted indoles and, because the starting materials are easy to make, it is particularly suitable for the synthesis of N(b)-di-substituted tryptamines (
Ian Fleming, Michael Woolias
openaire +1 more source
THE PHARMACOLOGY OF TRYPTAMINE
Australian Journal of Experimental Biology and Medical Science, 1951openaire +2 more sources
TRYPTAMINE TOXICITY IN ADRENALECTOMIZED RATS; ITS PREVENTION WITH TRYPTAMINE AND HYDROCORTISONE
The Journal of Pharmacology and Experimental Therapeutics, 1967W D, Denckla, H K, Dewey
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A qualitative descriptive analysis of effects of psychedelic phenethylamines and tryptamines
Human Psychopharmacology, 2020Joseph J Palamar, Patricia Acosta
exaly