Bulletin of the Korean Chemical Society

  • 제24권11호
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  • Pages.1632-1636
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  • 2003
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Synthesis of Neopentyl Biphenylsulfonates Using the Suzuki-Miyaura Reaction

  • Cho, Chul-Hee (Department of Chemical Engineering, Chung-Ang University) ;
  • Kim, Chul-Bae (Department of Chemical Engineering, Chung-Ang University) ;
  • Sun, Myung-Chul (Department of Chemical Engineering, Chung-Ang University) ;
  • Park, Kwang-Yong (Department of Chemical Engineering, Chung-Ang University)
  • 발행 : 2003.11.20
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초록

Palladium-catalyzed cross-coupling reactions of neopentyloxysulfonylphenyl bromides with arylboronic acids provided a variety of neopentyl biphenylsulfonates in good yields. 2-Bromo- and 4-bromobenzenesulfonates underwent the coupling reaction more rapidly than 3-bromobenzenesulfonate, while chlorobenzenesulfonate did not produce the coupling product under the standard reaction conditions.

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참고문헌

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피인용 문헌

  1. Synthesis of Neopentyl Biphenylsulfonates Using the Suzuki-Miyaura Reaction. vol.35, pp.16, 2004, https://doi.org/10.1002/chin.200416092
  2. Nickel-Catalyzed Coupling of Arenesulfonates with Primary Alkylmagnesium Halides vol.26, pp.9, 2005, https://doi.org/10.5012/bkcs.2005.26.9.1410
  3. Nickel-Catalyzed Hydrogenolysis of Arenesulfonates Using Secondary Alkyl Grignard Reagents vol.28, pp.2, 2003, https://doi.org/10.5012/bkcs.2007.28.2.281
  4. Parallel Synthesis of Unsymmetrical trans-Stilbenes vol.28, pp.7, 2007, https://doi.org/10.5012/bkcs.2007.28.7.1159