4.6 Article

Copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides

期刊

RSC ADVANCES
卷 6, 期 67, 页码 62298-62301

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra11301j

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资金

  1. National Natural Science Foundation of China [21401080, 51503086]
  2. Natural Science Foundation of Jiangsu Province of China [BK20130125]
  3. MOE for the 111 Project [B13025]
  4. SAFEA for the 111 Project [B13025]

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The efficient copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides has been developed under mild conditions with moderate to good yields. Significantly, this provides an alternative method to synthesise arylthioquinone derivatives. This is the first time that arylthioquinones with arylsulfonyl chlorides as starting material have been prepared, which avoids the use of the awful smelling thioalcohols and thiophenols.

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