Synthesis of trans-N,N,N-triethyl-2-ethanammonium iodide
The antispasmodic olefin trans-N,N,N-triethyl-2-ethanammonium iodide has been made by hydroalumination of a trimethylsilylalkyne followed by palladium-catalyzed cross-coupling of the vinylalane with the appropriate aryl bromide.
Synthesis of N,N,N-Triethyl-2-ethanammonium iodide.
The synthesis of N,N,N-triethyl-2-ethanammonium iodide, antispasmodic disubstituted olefin, was achieved via palladium-catalyzed cross-coupling of phenylacetylide with aryl bromide followed by hydroalumination.
Al-Hassan, Mohammed I.
p. 1677 - 1680
(2007/10/02)
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