REACTIONS OF ARYL HALIDES WITH THIOLATE ANIONS IN THE PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM PREPARATION OF ARYL SULFIDES
- 5 January 1978
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 7 (1) , 13-14
- https://doi.org/10.1246/cl.1978.13
Abstract
Aryl bromide and iodide were found to react with aliphatic and aromatic thiolate anions to give the corresponding sulfides in the presence of Pd(O). The reaction was not inhibited by p-dinitrobenzene which is a good inhibitor for the SRN1.This publication has 3 references indexed in Scilit:
- FACILE SYNTHESIS OF ARYL CYANIDES FROM IODIDES CATALYZED BY PALLADIUM TRIPHENYLPHOSPHINE COMPLEXChemistry Letters, 1975
- Nucleophilic replacement of two halogens in dihalobenzenes without the intermediacy of monosubstitution productsThe Journal of Organic Chemistry, 1974
- Nucleophilic aromatic substitutionTetrahedron Letters, 1973