Bibliographic Information

Heterocyclic chemistry

J.A. Joule, K. Mills, G.F. Smith

S. Thornes, 1998

3rd ed

Available at  / 2 libraries

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Description and Table of Contents

Description

Covering the fundamentals of heterocyclic reactivity and synthesis, this book teaches the subject in a way that is understandable to graduate students. Recognizing the level at which heterocyclic chemistry is often taught, the authors have included advanced material that make it appropriate for postgraduate courses. The text discusses the chemical reactivity and synthesis of particular heterocyclic systems. Exercises and solutions help students understand and apply the principles. Original references are included throughout, as well as many review references.

Table of Contents

Structures And Main Physical Properties Of Aromatic Heterocycles, Reactivity Of Aromatic Heterocycles, Synthesis Of Aromatic Heterocycles, Typical Reactivity Of Pyridines, Quinolines, And Isoquinolines, Pyridines: Reactions And Synthesis, Quinolines And Isoquinilines: Reactions And Synthesis, Typical Reactivity Of Pyrylium And Benzopyrylium Ions, Pyrones, And Benzopyrones, Pyryliums, 2- And 4-Pyrones: Reactions And Synthesis, Benzopyryliums And Benzopyrones: Reactions And Synthesis, Typical Reactivity Of The Diazines: Pyridazine, Pyrimidine, And Pyrazin, The Diazines: Pyridazine, Pyrimidine, And Pyrazine: Reactions And Synthesis, Isoindoles, Benzo[C]Thiopenes And Isobenzofurans: Reactions And Synthesis, Typical Reactivity Of 1,3,- And 1,2-Azoles: Reactions And Synthesis, 1,2-Azoles:Pyrazoles, Isothiazoles, And Isoxazoles: Reactions And Synthesis, Purines: Reactions And Synthesis, Heterocycles Containing A Ring-Junction Nitrogen, Heterocycles Containing More Than Two Hetero Atoms

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Details

  • NCID
    BA45638164
  • ISBN
    • 0748740694
  • Country Code
    uk
  • Title Language Code
    eng
  • Text Language Code
    eng
  • Place of Publication
    Cheltenham
  • Pages/Volumes
    xviii, 516 p.
  • Size
    24 cm
  • Classification
  • Subject Headings
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