Preface
Journals Abstracted
Glossary of Abbreviations
I. Carbon-Carbon Bond Forming Reactions
Carbon-Carbon Single Bonds (See Also: I.E., I.F, I.G)
1. Alkylation of Aldehydes, Ketones, and their Derivatives
2. Alkylations of Nitriles, Acids, and Acid Derivatives
3. Alkylation of ß-Dicarbonyl and ß-Cyanocarbonyl Systems and Other Active Methylene Compounds
4. Alkylation of N-, S-, and Se-Stabilized Carbanions
5. Alkylation of Organometallic Reagents (See Also: I.F, I.G)
6. Other Alkylation Procedures and Reviews
7. Nucleophilic Addition to Electron-Deficient Carbon
8. Other Carbon-Carbon Single Bond Forming Reactions
B. Carbon-Carbon Double Bonds (See Also: I.E.1, III.G, VI.A.16)
1. Wittig-Type Olefination Reactions
2. Eliminations
3. Other Carbon-Carbon Double Bond Forming Reactions
4. Allene Forming Reactions
C. Carbon-Carbon Triple Bonds (See Also: VI.A.16)
D. Cyclopropanations
1. Carbene or Carbenoic Additions to a Multiple Bond (See Also: VI.A.7)
2. Other Cyclopropanations
Ε. 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
3. Other Aromatic Substitutions
G. Synthesis via Organometallics
1. Organoboranes
2. Carbonylation Reactions
3. Other Synthesis via Organometallics
4. Reviews
II. Oxidations
A. C-O Oxidations
1. Alcohol → Ketone, Aldehyde
2. Alcohol, Aldehyde → Acid, Acid Derivative
B. C-H Oxidations
1. C-H → C-O
2. C-H → C-Hal
3. Other C-H Oxidations
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. Phenol → Quinone Oxidation
H. Oxidative Cleavages
I. Photosensitized Oxygenations
J. Dehydrogenation
K. Other Oxidations and Reviews
III. Reductions
A. C = O Reductions (See Also: III.F.1)
Β. C-N Multiple Bond Reductions
1. Nitrile Reductions
2. Imine Reductions
C. Reduction of Sulfur Compounds
D. N-O Reductions
Ε. C-C Multiple Bond Reductions
1. C = C Reductions
2. C ≡ C Reductions
3. Reduction of Aromatic Rings
F. Hydrogenolysis of Hetero Bonds
1. C-O → C-H
2. C-Hal → C-H
3. C-S → C-H
4. C-N → C-H
G. Reductive Eliminations
H. Reductive Cleavages
I. Hydroboration (Reduction Only)
J. Other Reductions and Reviews
IV. Synthesis of Heterocycles
A. Aziridines
B. Furans, etc
C. Indoles
D. Lactams
E. Lactones
F. Pyridines, Quinolines, etc
G. Pyrroles, etc
H. Other Heterocycles with One Heteroatom (See Also: II.F.1, VI.A.9)
I. Heterocycles with Two or More Heteroatoms
1. Heterocycles with 2 Ns
2. Heterocycles with 1 Ν and 1 O
3. Heterocycles with 1 Ν and 1 S
4. Heterocycles with 1 S and 1 O
5. Heterocycles with 3 Ns
6. Other Heterocycles
J. General Reviews
V. Protecting Groups
A. Hydroxyl(See Also: VI.A.10, VI.A.11)
B. Amine (See Also: VI.A.4)
C. Sulfhydryl (See Also: VI.A.19)
D. Carboxyl (See Also: VI.A.4, VI.A.10)
E. Ketone, Aldehyde (See Also: VI.A.18)
F. Phosphate
G. Pi Bond
H. Miscellaneous Protecting Groups
VI. Useful Synthetic Preparations
A. Functional Group Preparations
1. Acids, Acid Halides, Anhydrides (See Also: II.A.2)
2. Alcohols, Phenols (See Also: II.B.1, III.Α., III.F.1)
3. Alkyl, Aryl Halides (See Also: II.B.2)
4. Amides(See Also: IV.D, VI.A.17)
5. Amines (See Also: III.B.2, III.D)
6. Amino Acids and Derivatives (See Also: III.E.1, VI.A.4, VI.A.10)
7. Carbenes (See Also: I.D)
8. Enamines
9. Epoxides (See Also: II.F.1, IV.H)
10. Esters (See Also: IV.E, V.D)
11. Ethers (See Also:· V.A)
12. Ketones and Aldehydes (See Also: I.A.2, II.A.1, III.F.1)
13. Nitriles
14. Nitro
15. Nucleotides, etc. (See Also: IV.I.1a, b, V.F)
16. Olefins, Acetylenes (See Also: I.B, I.C, II.J, III.G)
17. Peptides (See Also: V.B, V.C, V.D, VI.A.4)
18. Vinyl Halides, Vinyl Ethers, Vinyl Esters
19. Sulfur Compounds (See Also: II.Ε, III.C)
B. Ring Enlargement and Contraction
1. Enlargement
2. Contraction
C. Multistep Transformations
1. Masked Carbonyl Systems
2. Other Multistep Transformations
VII. Miscellaneous Reviews
Author Index