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The application of cyclobutane derivatives in organic synthesis

  • Henry N. C. Wong
  • Kin-Lik Lau
  • Kam-Fai Tam
Conference paper
Part of the Topics in Current Chemistry book series (TOPCURRCHEM, volume 133)

Abstract

A great variety of methods are available for the synthesis of cyclobutane derivatives. These methods generally allow regioselective as well as stereoselective synthesis of extensively substituted four-membered ring carbocycles. Although possessing intense ring strain, cyclobutanes are normally stable at room temperature, hence can be handled easily in laboratories. Nevertheless, four-membered ring compounds can undergo ring cleavage with extreme ease under several reaction conditions such as acidic condition, basic condition, nucleophilic attack, thermolysis, photolysis, oxidizing as well as reducing conditions. When the cyclobutane ring under investigation is appropriately designed to link to other functional groups, ring opening can be usually followed by skeletal rearrangement. These intriguing reactions would yield compounds with very complex structures. Therefore, the combined effect of all these special properties enables cyclobutane derivatives to become very versatile and useful starting materials for organic synthesis.

Keywords

Organic Synthesis Ring Opening Total Synthesis Ring Expansion Olefin Metathesis 
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.

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Copyright information

© Springer-Verlag 1986

Authors and Affiliations

  • Henry N. C. Wong
    • 1
  • Kin-Lik Lau
    • 2
  • Kam-Fai Tam
    • 2
  1. 1.Department of ChemistryThe Chinese University of Hong KongHong Kong
  2. 2.Department of Applied ScienceHong Kong PolytechnicHong Kong

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