Literature DB >> 17851422

Fast and highly efficient solid state oxidation of thiols.

Morteza Montazerozohori1, Shiva Joohari, Bahador Karami, Nasrin Haghighat.   

Abstract

A fast and efficient solid state method for the chemoselective room temperature oxidative coupling of thiols to afford their corresponding disulfides using inexpensive and readily available moist sodium periodate as the reagent is described. The reaction was applicable to a variety of thiols giving high yields after short reaction times. Comparison of yield/time ratios of this method with some of those reported in the literature shows the superiority of this reagent over others under these conditions.

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Year:  2007        PMID: 17851422      PMCID: PMC6149396          DOI: 10.3390/12030694

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  2 in total

1.  Peptide bond formation mediated by 4,5-dimethoxy-2-mercaptobenzylamine after periodate oxidation of the N-terminal serine residue.

Authors:  T Kawakami; K Akaji; S Aimoto
Journal:  Org Lett       Date:  2001-05-03       Impact factor: 6.005

2.  Urea- hydrogen peroxide (UHP) oxidation of thiols to the corresponding disulfides promoted by maleic anhydride as mediator.

Authors:  Bahador Karami; M Montazerozohori; M H Habibi
Journal:  Molecules       Date:  2005-10-31       Impact factor: 4.411

  2 in total
  1 in total

1.  Inhibition of biofilm formation, quorum sensing and infection in Pseudomonas aeruginosa by natural products-inspired organosulfur compounds.

Authors:  Nathaniel C Cady; Kurt A McKean; Jason Behnke; Roman Kubec; Aaron P Mosier; Stephen H Kasper; David S Burz; Rabi A Musah
Journal:  PLoS One       Date:  2012-06-08       Impact factor: 3.240

  1 in total

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