Preface
Journals Abstracted
I. Carbon-Carbon Bond Forming Reactions
A. Carbon-Carbon Single Bonds (See Also: Thermal Reactions 126, Aromatic Substitutions Forming a New Carbon—Carbon Bond 135, Photochemical Reactions 148)
1. Alkylation of Aldehydes, Ketones and Their Derivatives (See Also: Nucleophilic Addition to Electron Deficient Carbon 34)
2. Alkylation of Acids and Acid Derivatives
3. Alkylation of ß-Dicarbonyl and ß-Cyanocarbonyl Systems
4. Alkylation of Organometallic Reagents (See Also: Aromatic Substitutions-Coupling Reactions 143)
5. Other Alkylation Procedures
6. Nucleophilic Addition to Electron Deficient Carbon
7. Carbonylation Procedures
8. Other Carbon-Carbon Single Bond Forming Reactions
B. Carbon-Carbon Double Bonds (See Also: Reductive Eliminations 177)
1. Wittig-Type Olefination Reactions
2. Eliminations
3. Other Carbon-Carbon Double Bond Forming Reactions
4. Allene Forming Reactions
C. Carbon-Carbon Triple Bonds
D. Cyclopropanations
1. Carbene or Carbenoid Addition to a Multiple Bond
2. Other Cyclopropanations
E. Thermal Reactions
1. Cycloadditions
2. Other Thermal Reactions
F. Aromatic Substitutions Forming a New Carbon-Carbon Bond
1. Friedel-Crafts-Type Reactions
2. Coupling Reactions (See Also: Synthesis via Organometallics 148)
3. Other Aromatic Substitutions
G. Photochemical Reactions
H. Synthesis via Organometallics
1. Organoboranes
2. Coupling Reactions
3. Other
4. Reviews
II. Oxidations
A. C-O Oxidations
1. Alcohol → Cetone, Aldehyde
2. Aldehyde → Acid, Ester, Amide
B. C-H Oxidations
1. Allylic C-H Bonds
2. C-H Bonds α to Carbonyl
3. C-H Bonds α to Sulfur
C. C-N Oxidations
D. Amine Oxidations
E. Sulfur Oxidations
F. Oxidative Additions to C—C Multiple Bonds
1. Epoxidations
2. Hydroxylation
3. Other
G. Halogenation of Aromatic Rings
H. Oxidative Cleavages
1. C-C Single Bonds
2. C-C Multiple Bonds
I. Photosensitized Oxygenations
J. Dehydrogenation
K. Phenol → Quinone Oxidation
L. Other Oxidations
M. New Procedures for Oxidation and Oxidation Reagents
III. Reductions
A. C=O Reductions
B. Nitrile Reductions
C. Reduction of Sulfur Compounds
D. N-O Reductions
E. C-C Multiple Bond Reductions
1. C=C Reductions
2. C≡C Reductions
3. Reduction of Aromatic Rings
F. Hydrogenolysis of C-Hetero Bonds
1. C-O → C-H
2. C-Hal → C-H
3. C=O → CH2
G. Reductive Eliminations
H. Reductive Cleavages
I. Hydroboration (Reduction Only)
J. Other Reductions
K. Reviews
IV. Synthesis of Heterocyclics
A. Aziridines
B. Furans
C. Indoles
D. Lactams
E. Lactones
F. Pyridines
G. Pyrroles and Pyrrolines
H. Quinolines and Isoquinolines
I. Other Heterocycles with One Heteroatom
J. Other Heterocycles
K. Reviews
V. Protecting Groups
A. Hydroxyl
B. Amine
C. Sulfhydryl
D. Carboxyl
E. Ketone, Aldehyde
F. Phosphate
VI. Useful Synthetic Preparations
A. Functional Group Preparations
1. Acids
2. Alcohols (See Also: Reduction of Carbonyls 169)
3. Alkyl Halides
4. Amides
5. Amines (See Also: Amide Reduction 101, Nitrile Reduction 170)
6. Amino Acids
7. Anhydrides
8. Arynes
9.Carbenes
10. Diazoalkanes
11. Enamines
12.Episulfides
13. Epoxides (See Also: Oxidative Addition to C=C 161)
14. Esters
15. Ethers
16. Isocyanates
17. Isocyanides
18. Ketones and Aldehydes (See Also: C-0 Oxidations 155)
19. ß-Dicarbonyl Compounds
20. Nitriles
21. Nitro
22. Nucleotides (See Also: Hydroxyl 189, Phosphate 194 Protecting Groups)
23. Peptides (See Also: Hydroxyl 189, Amine 190 Protecting Groups)
24. Phenols
25. Phosphates
26. Vinyl Halides, Vinyl Ethers, Vinyl Esters
B. Multi-Step Transformations
1. Ring Enlargement
2. Masked-Carbonyl Systems
3. Organoboranes (See Also: Synthesis via Organometallics 148)
4. Other
VII. Other Completely Miscellaneous Reactions
VIII. Miscellaneous Reviews