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Efficient and Facile Synthesis of α-Chloroenones Bearing β-Carbonates or β-Carbamates

  • Received : 2012.09.05
  • Accepted : 2012.10.04
  • Published : 2012.12.20

Abstract

Efficient synthesis of ${\alpha}$-chloroenones bearing ${\beta}$-carbonates or ${\beta}$-carbamates was achieved by rhodium(II)-catalyzed reaction of cyclic diazodicarbonyl compounds with a variety of chloroformates or carbamyl chlorides in good yields. These reactions provided a useful and rapid route to ${\beta}$-substituted ${\alpha}$-haloenones.

Keywords

References

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피인용 문헌

  1. Designs and Strategies for the Halo-Functionalization of Diazo Compounds vol.360, pp.17, 2018, https://doi.org/10.1002/adsc.201800340
  2. Regioselective Synthesis of Highly Functionalized Furans Through the RuII‐Catalyzed [3+2] Cycloaddition of Diazodicarbonyl Compounds vol.2014, pp.16, 2012, https://doi.org/10.1002/ejoc.201402067