The Journal of Organic Chemistry

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

Full Text: HTML

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 ...

Related Articles:

Disulfides as efficient thiolating reagents enabling selective bis-sulfenylation of aryl dihalides under mild copper-catalyzed conditions

[Liu, Yunyun; Wang, Hang; Zhang, Jida; Wan, Jie-Ping; Wen, Chengping RSC Advances, 2014 , vol. 4, # 37 p. 19472 - 19475]

A convenient s rn 1 synthesis of aromatic nitriles from diazonium salts via diazosulfides

[Petrillo, Giovanni; Novi, Marino; Garbarino, Giacomo; Dell'erba, Carlo Tetrahedron, 1987 , vol. 43, # 20 p. 4625 - 4634]

A mild and efficient SRN1 approach to diaryl sulfides from arenediazonium tetrafluoroborates

[Petrillo, Giovanni; Novi, Marino; Garbarino, Giacomo; Dell'Erba, Carlo Tetrahedron, 1986 , vol. 42, # 14 p. 4007 - 4016]

A convenient s rn 1 synthesis of aromatic nitriles from diazonium salts via diazosulfides

[Petrillo, Giovanni; Novi, Marino; Garbarino, Giacomo; Dell'erba, Carlo Tetrahedron, 1987 , vol. 43, # 20 p. 4625 - 4634]

Reduction of Disulfides with Copper. Preparation of Some Thioethers

[Campbell,J.R. Journal of Organic Chemistry, 1962 , vol. 27, p. 2207 - 2209]

More Articles...