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Thiol-free chemoenzymatic synthesis of β-ketosulfides.

Adrián A HerediaMartín G López-VidalMarcela Kurina-SanzFabricio R BisognoAlicia B Peñéñory
Published in: Beilstein journal of organic chemistry (2019)
A preparation of β-ketosulfides avoiding the use of thiols is described. The combination of a multicomponent reaction and a lipase-catalysed hydrolysis has been developed in order to obtain high chemical diversity employing a single sulfur donor. This methodology for the selective synthesis of a set of β-ketosulfides is performed under mild conditions and can be set up in one-pot two-step and on a gram-scale.
Keyphrases
  • gram negative
  • mass spectrometry
  • multidrug resistant
  • anaerobic digestion
  • high resolution
  • tandem mass spectrometry