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Thiols, arylation

Cuprous oxide, in thiol arylation, 50, 75 Curtius reaction, modiflcation using mixed carboxylic-carbonic aidiy-drides, 51, 51... [Pg.73]

Boots, A.W., Haenen, G.R., den Hartog, G.J., and Bast, A., Oxidative damage shifts from lipid peroxidation to thiol arylation by catechol-containing antioxidants, Biochim. Biophys. Acta, 1583, 279, 2002. [Pg.369]

Benzene thiol arylation with bromobenzene was reported by Foa et al. utilizing a biphasic aqueous-toluene system (Scheme 3.5) [12]. [Pg.71]

In 2009, Reddy et al. [150] reported the use of a nano-indium oxide as a recyclable catalyst for the ligand-free thiol arylation with both aryl bromides and iodides. The specific conditions were In Oj nanoparticles (3 mol%) and KOH (2 equiv) in DMSO for 24 h at 135 ° C. The scope was clearly demonstrated affording high yields of the product. The catalyst could be recovered by ultracentrifugation and reused up to four times without much loss in activity. [Pg.141]


See other pages where Thiols, arylation is mentioned: [Pg.214]    [Pg.77]    [Pg.49]    [Pg.1918]    [Pg.214]    [Pg.71]    [Pg.14]    [Pg.95]    [Pg.96]    [Pg.98]    [Pg.100]    [Pg.102]    [Pg.104]    [Pg.106]    [Pg.108]    [Pg.110]    [Pg.112]    [Pg.114]    [Pg.116]    [Pg.118]    [Pg.120]    [Pg.122]    [Pg.124]    [Pg.126]    [Pg.128]    [Pg.130]    [Pg.132]    [Pg.134]    [Pg.138]    [Pg.140]    [Pg.141]    [Pg.142]    [Pg.143]    [Pg.144]    [Pg.144]    [Pg.146]   
See also in sourсe #XX -- [ Pg.100 , Pg.241 , Pg.242 , Pg.243 ]




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Arylation of thiols

Catalyzed Reactions of Aryl Halides with Thiols

Copper-Catalyzed Coupling of Aryl Halides with Amines, Alcohols, and Thiols

Copper-Catalyzed Thiol Arylation

Cuprous oxide, in thiol arylation

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Thiols from aryl halides

Thiols, aryl

Thiols, aryl coupling reactions

Thiols, aryl halides

Thiols, aryl with Grignard reagents

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