1962
DOI: 10.1021/jo01057a032
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Oxidation of Monomeric and Polymeric Sulfhydryl Compounds1

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Cited by 19 publications
(6 citation statements)
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“…In a similar fashion already reported in literature for the synthesis of GSH-and NAC-CS and GC polymer conjugates [9], [10], [16], GSH-and NAC-GC thiomers were obtained by the formation of amide bonds between primary amino groups linked to the C-2 of pyranose ring of GC backbone and glycine carboxylic acid groups or cysteine carboxylic acid groups of GSH and NAC, respectively. Thiol groups of polymers, and other thiols in the proteins, can be oxidized to disulfides in aqueous solutions by intra-and/or intermolecular reactions [23], [24]. The pH affected the oxidation lability of thiol groups.…”
Section: Synthesis Of Gsh-and Nac-gc Polymer Conjugatesmentioning
confidence: 99%
“…In a similar fashion already reported in literature for the synthesis of GSH-and NAC-CS and GC polymer conjugates [9], [10], [16], GSH-and NAC-GC thiomers were obtained by the formation of amide bonds between primary amino groups linked to the C-2 of pyranose ring of GC backbone and glycine carboxylic acid groups or cysteine carboxylic acid groups of GSH and NAC, respectively. Thiol groups of polymers, and other thiols in the proteins, can be oxidized to disulfides in aqueous solutions by intra-and/or intermolecular reactions [23], [24]. The pH affected the oxidation lability of thiol groups.…”
Section: Synthesis Of Gsh-and Nac-gc Polymer Conjugatesmentioning
confidence: 99%
“…Even molecular oxygen will oxidize thiols in the presence of trace amounts of metal ions [98]. The nature of neighbouring groups greatly influences the oxidation of thiols [99]. The side chains of His, Tyr, Met, Cys and Trp residues can be oxidized via photo-oxidation in the presence of dyes [96].…”
Section: Other Residuesmentioning
confidence: 99%
“…Oxidation of thiol groups to the disulfide was, for example, investigated by Barron et al 37) and by Overberger and Ferraro. 38) They demonstrated that the oxidizability of dithiols increases as the distance between the thiol groups decreases. Negishi and Tsukuda synthesized gold clusters using the oxidation of a dithiol: meso-2,3-dimercaptosuccinic acid.…”
Section: Growth Of Gold Using Mptms As a Reducing Agentmentioning
confidence: 99%