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Name Reactions pp 275-276 | Cite as

Mukaiyama esterification

  • Jie Jack Li

Abstract

Esterification using Mukaiyama reagent such as 2-chloro-1-methyl-pyridinium iodide (Mukaiyama reagent).

Keywords

Inorganic Chemistry Organic Chemistry General Scheme Mechanistic Pathway Amide Formation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. 1.
    Mukaiyama, T.; Usui, M.; Shimada, E.; Saigo, K. Chem. Leu. 1975, 1045.Google Scholar
  2. 2.
    Hojo, K.; Kobayashi, S.; Soai, K.; Ikeda, S.; Mukaiyama, T. Chem. Lett. 1977, 635.Google Scholar
  3. 3.
    Mukaiyama, T. Angew. Chem., Ina. Ed. Engl. 1979, 18, 707.CrossRefGoogle Scholar
  4. 4.
    For amide formation, see: Huang, H.; Iwasawa, N.; Mukaiyama, T. Chem. Leu. 1984, 1465.Google Scholar
  5. 5.
    Nicolaou, K. C.; Bunnage, M. E.; Koide, K. J. Am. Chem. Soc. 1994, 116, 8402.CrossRefGoogle Scholar
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    Yong, Y. F.; Kowalski, J. A.; Lipton, M. A. J. Org. Chem. 1997, 62, 1540.CrossRefGoogle Scholar
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    Folmer, J. J.; Acero, C.; Thai, D. L.; Rapoport, H. J. Org. Chem. 1998, 63, 8170.CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2003

Authors and Affiliations

  • Jie Jack Li
    • 1
  1. 1.Chemistry DepartmentPfizer Global Research and DevelopmentAnn ArborUSA

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