The Journal of organic chemistry

Transition-Metal-Free Acid-Mediated Synthesis of Aryl Sulfides from Thiols and Thioethers

AM Wagner, MS Sanford

Index: Wagner, Anna M.; Sanford, Melanie S. Journal of Organic Chemistry, 2014 , vol. 79, # 5 p. 2263 - 2267

Full Text: HTML

Citation Number: 22

Abstract

One of the most common routes to aryl sulfides involves the transition-metal-catalyzed cross-coupling of aryl halides or pseudo-halides with thiols under basic conditions.(11-16) A number of base-mediated, transition-metal-free reactions for aryl sulfide synthesis have also been reported.(17-25) While these represent highly useful transformations, the vast majority of current synthetic methods for aryl sulfide synthesis require at least one of the following: ...

Related Articles:

Triethyl phosphite in organic synthesis. A facile, one-pot conversion of alcohols into amines

[Zwierzak, Andrzej Phosphorus, Sulfur and Silicon and the Related Elements, 1993 , vol. 75, # 1-4 p. 51 - 54]

Synthesis of cis and trans Whisky and Cognac lactones by the regiocontrolled alkylation of 2??(trimethylsiloxy) furan

[Jefford, Charles W.; Sledeski, Adam W.; Boukouvalas, John Helvetica Chimica Acta, 1989 , vol. 72, p. 1362 - 1370]

Reaction of trifluoroacetic acid with alcohols, phenols, ethers, and their sulfur analogs

[Hagen, Arnulf P.; Miller, Tammy S.; Bynum, Richard L.; Kapila Ved P. Journal of Organic Chemistry, 1982 , vol. 47, # 7 p. 1345 - 1347]

Homogeneous catalytic oxidation of light alkanes: CC bond cleavage under mild conditions

[Chepaikin; Bezruchenko; Menchikova; Moiseeva; Gekhman Kinetics and Catalysis, 2010 , vol. 51, # 5 p. 666 - 671]

Synthesis of cis and trans Whisky and Cognac lactones by the regiocontrolled alkylation of 2??(trimethylsiloxy) furan

[Jefford, Charles W.; Sledeski, Adam W.; Boukouvalas, John Helvetica Chimica Acta, 1989 , vol. 72, p. 1362 - 1370]

More Articles...