Side Reactions in Organic Synthesis II: Aromatic Substitutions

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Side Reactions in Organic Synthesis II
Cover
Related Titles
Title Page
Copyright
Preface
Glossary and Abbreviations
Journal Abbreviation List
Chapter 1: Electrophilic Alkylation of Arenes
1.1 General Aspects
1.2 Problematic Arenes
1.3 Problematic Electrophiles
References
Chapter 2: Electrophilic Olefination of Arenes
2.1 General Aspects
2.2 Olefinations with Leaving-Group-Substituted Olefins
2.3 Olefinations with Unsubstituted Olefins
2.4 Olefinations with Alkynes
References
Chapter 3: Electrophilic Arylation of Arenes
3.1 General Aspects
3.2 Arylations with Aryl Halides
3.3 Arylations with Diazonium Salts
3.4 Arylations with Other Functionalized Arenes
3.5 Arylations with Unsubstituted Arenes
References
Chapter 4: Electrophilic Acylation of Arenes
4.1 General Aspects
4.2 Problematic Arenes
4.3 Problematic Electrophiles
References
Chapter 5: Electrophilic Halogenation of Arenes
5.1 General Aspects
5.2 Typical Side Reactions
5.3 Regioselectivity
5.4 Catalysis
5.5 Fluorinations
5.6 Electron-Deficient Arenes
5.7 Electron-Rich Arenes
5.8 Sensitive Functional Groups
References
Chapter 6: Electrophilic Formation of Aromatic C–N Bonds
6.1 Nitration of Arenes
6.2 Electrophilic Aromatic Aminations
6.3 Electrophilic Aromatic Amidations
References
Chapter 7: Electrophilic Formation of Aromatic C–S Bonds
7.1 Sulfonylation
7.2 Sulfinylation
7.3 Sulfenylation
References
Chapter 8: Aromatic Nucleophilic Substitutions
8.1 General Aspects
8.2 Problematic Electrophiles
8.3 Problematic Nucleophiles
References
Epilogue Economics, Politics, and the Quality of Chemical Research
Prosperity
Slavery and Freedom
The Quality of Chemical Research
References
Index
End User License Agreement
Pages