Synthesis of thioethers. Amide solvent-promoted nucleophilic displacement of halide by thiolate ion
JR Campbell
Index: Campbell,J.R. Journal of Organic Chemistry, 1964 , vol. 29, p. 1830 - 1833
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Citation Number: 90
Abstract
Methods for the preparation of aryl thioethers have generally suffered from limited applicability in that activated reactants, severe reaction conditions, complicated procedures, or a combination of these requirements were Parker6 has stated that unsymmetrical aryl sulfides can be prepared in high yields providing the halogen substrate is activated by at least one powerful electron-u ithdrawing substituent. A recent method7 developed in ...
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