4.8 Article

Efficient Access to 1,4-Benzothiazine: Palladium-Catalyzed Double C-S Bond Formation Using Na2S2O3 as Sulfurating Reagent

Journal

ORGANIC LETTERS
Volume 15, Issue 11, Pages 2594-2597

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol400618k

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Funding

  1. NSFC [21272075]
  2. NCET [12-0178]
  3. Shanghai Pujiang Program [12PJ1402500]
  4. Shanghai Talent Development Support [2011022]
  5. CPSF [2012M520858]

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A novel Pd-catalyzed double C-S bond formation coupling reaction has been developed. This protocol, in which Na2S2O3 was used as sulfurating reagent in metal-catalyzed reactions, provides an efficient method for the synthesis of substituted 1,4-benzothiazine derivates, which are structural elements of numerous bioactivity molecules rendering this protocol attractive to both synthetic and medicinal chemistry.

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