6268-31-1Relevant articles and documents
Nonisocyanate route to 2,5-bis(hydroxymethyl)furan-based polyurethanes crosslinked by reversible diels–alder reactions
Zhang, Lu,Michel, Frederick C.,Co, Anne C.
, p. 1495 - 1499 (2019)
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Efficient and Green Preparation of 2-Imidazolidinone using Sulfamic Acid as Acidic Catalyst
Liu, Jianshe,Xie, Yaqiang,Ye, Liyi,Yan, Huidong,Tu, Song
, p. 453 - 456 (2015/10/28)
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Synthesis of Dithiols as Reducing Agents for Disulfides in Neutral Aqueous Solution and Comparison of Reduction Potentials
Lamoureux, Guy V.,Whitesides, George M.
, p. 633 - 641 (2007/10/02)
Several dithiols have been prepared that are useful for the reduction of disulfides in aqueous solution.The reduction potential of these thiols have been determined from the measurement of the equilibrium constant of thiol/disulfide interchange with oxidized dithiothreitol using a 1H NMR assay.The values of pKa of some of the dithiols were measured to estimate their rate of reduction of disulfides.Bis(2-mercaptoethyl) sulfone (2), N,N'-dimethyl-N,N'-bis(mercaptoacetyl)hydrazine (5), and meso-2,5-dimercapto-N,N,N',N'-tetramethyladipamide (6) are especially interesting as alternatives to dithiothreitol for the reduction of disulfides.