147591-61-5Relevant academic research and scientific papers
(Cyanomethyl)trimethylphosphonium iodide as reagent for the intermolecular S-alkylation of thiols with alcohols
Zaragoza
, p. 5451 - 5454 (2001)
Treatment of mixtures of thiols and primary aliphatic alcohols with (cyanomethyl)trimethylphosphonium iodide leads to the clean formation of unsymmetric thioethers. The required phosphonium iodide is simple to prepare and stable towards air and moisture.
Synthesis, spectral studies and C-S, C-N bond fissions of some novel N-[alkyl (4′-substituted phenylthio)] phthalimides
El-Bardan, Ali A.
, p. 511 - 519 (2007/10/03)
N-[(4′-Substituted phenylthio)ethyl] phthalimide la-g and their corresponding n-propyl 2a-g, n-butyl 3a-g derivatives have been synthesised. The structure of these compounds were proved by UV, IR, 1H NMR, 13CMR and mass spectra. The 1H and 13C chemical shifts of the adjacent methylene protons and carbons of both the sulfur atom and phthalimido nitrogen group were reasonably correlated using σ° values. The carbon-nitrogen and the carbon-sulfur bond fissions in alkaline and acidic media were discussed.
INDOLE DERIVATIVES. 138. SYNTHESIS OF α-(5-INDOLYL)ETHYLAMINE AND 5-(2-AMINOETHOXY)- AND 5-(AMINOETHYLTHIO)TRYPTAMINES
Gordeev, E. N.,Buyanov, V. N.,Zhigachev, V. E.
, p. 40 - 42 (2007/10/02)
The reaction of 5-acetylindole with hydroxylamine with subsequent reduction of the resulting oxime gave α-(5-indolyl)ethylamine.Coupling of 4-(2-phthalimidoethoxy)- and 4-(2-phthalimidoethylthio)phenyldiazonium chlorides with ethyl α-acetyl-δ-phthalimidov
