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Functional Group Interconversion by Nucleophilic Substitution

  • Francis A. Carey
  • Richard J. Sundberg
Part of the Advanced Organic Chemistry book series

Abstract

The first two chapters have dealt with formation of new carbon bonds by processes in which carbon is the nucleophilic atom. The reactions considered in Chapter 1 involve attack by carbon nucleophiles at sp 3 centers, while those discussed in Chapter 2 involved reaction at sp 2 centers, primarily carbonyl groups. In this chapter we turn our attention to noncarbon nucleophiles. Nucleophilic substitution both at sp 3 and sp 2 centers is used in a variety of synthetic operations, particularly in the interconversion of functional groups. The mechanistic aspects of these reactions are treated more fully in Part A, Chapters 5 and 8.

Keywords

Crown Ether Acid Chloride Nucleophilic Substitution Alkyl Halide Thionyl Chloride 
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 Science+Business Media New York 1983

Authors and Affiliations

  • Francis A. Carey
    • 1
  • Richard J. Sundberg
    • 1
  1. 1.University of VirginiaCharlottesvilleUSA

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