Annual Reports in Organic Synthesis - 1971

Annual Reports in Organic Synthesis - 1971 presents a collection of 49 abstracted chemistry journals that cover organic synthesis. This book is comprised of eight chapters that cover different aspects of organic synthesis, such as reaction types and methods.
The first three chapters tackle carbon-carbon bond forming reactions, oxidations, and reductions. Chapter IV discusses synthesis of heterocyclics, and Chapter V covers the use of protecting groups. Chapter VI talks about useful synthetic preparations. Chapters VII and VIII cover the miscellaneous reactions and reviews.
The information provided by this text will be most useful to organic chemists.

Contenu

Preface

Journals Abstracted

I. Carbon-Carbon Bond Forming Reactions

A. Carbon-Carbon Single Bonds (See Also: Thermal Reactions 134, Photochemical Reactions 164)

1. Alkylation of Aldehydes and Ketones (See Also: Nucleophilic Addition to Electron Deficient Carbon 26)

2. Alkylation of Acids and Esters

3. Alkylation of ß-Dicarbonyl and ß-Cyanocarbonyl Systems

4. Alkylation of Nitriles

5. Other Alkylation Procedures

6. Nucleophilic Addition to Electron Deficient Carbon

7. Other Carbon-Carbon Single Bond Forming Reactions

   B. Carbon-Carbon Double Bonds (See Also: Reductive Eliminations 221)

8. Wittig-Type Olefination Reactions

9. Eliminations

10. Other Carbon-Carbon Double Bond Forming Reactions

11. Aliene Forming Reactions

    C. Carbon-Carbon Triple Bonds

    D. Cyclopropanations

12. Carbene or Carbenoid Addition to a Double Bond

13. Other

    . Thermal Reactions

14. Cycloadditions

15. Other Thermal Reactions

    F. Aromatic Substitutions Forming a New Carbon-Carbon Bond

16. Friedel-Crafts-Type Reactions

17. Phenol Coupling

18. Other

    G. Photochemical Reactions

19. Enone + Olefin Cycloadditions

20. Photocyclizations

21. Other

22. Reviews

    H. Synthesis via Organometallics

23. Organoalanes

24. Organoboranes

25. Hydrosilylation

26. Coupling Reactions

27. Carbonylations and Decarbonylations

28. Olefin Oligomerizations

29. Metalations

30. Other

31. Reviews

II. Oxidations

A. C-O Oxidations

1. Alcohol Ketone, Aldehyde

2. Alcohol Acid, Ester

3. Aldehyde Acid, Ester, Amide

   B. C-H Oxidations

   1.Allylic C-H Bonds

4. Benzylic C-H Bonds

5. Remote C-H Bonds

6. C-H Bonds a to Oxygen or Nitrogen

7. C-H Bonds a to Carbonyl

8. C-H Bonds a to Sulfur

   C. C-Hetero Oxidations Other than C-H and C-O

9. C-N Oxidations

10. Other

    D. Amine Oxidations

    E. Sulfur Oxidations

    F. Oxidative Additions to C-C Multiple Bonds

11. Halohydrin Formation

12. Epoxidation

13. Halogenation

14. Hydroxylation

15. Other

    G. Oxidative Substitution on Aromatic Rings

16. Halogenation

17. Hydroxylation

18. Other

    H. Oxidative Cleavages

19. C-C Single Bonds

20. C-C Multiple Bonds

    L. Photosensitized Oxygenation

    J. Dehydrogenation

    K. Phenol Quinone Oxidation

    L. Other Oxidations

    M. New Procedures for Preparing Oxidation Reagents

    N. Reviews

III. Reductions

A. C=O Reductions

1. Ketone, Aldehyde Reductions

2. Acid, Anhydride, Acid Chloride Reductions

3. Ester, Lactone Reductions

4. Amide, Lactam Reductions

   . C-N Multiple Bond Reductions

5. Oxime Reductions

6. Nitrile Reductions

7. Other

   C. Reduction of Sulfur Compounds

   D. N-O Reductions

   E. C-C Multiple Bond Reductions

8. C=C Reductions

9. C=C Reductions

10. Reduction of Aromatic Rings

    F. Hydrogenolysis of C - Hetero Bonds

    l. C-O C-H

11. C-Hal C-H

12. C-S C-H

13. C=O CH2

14. Other

    G. Reductive Eliminations

    H. Reductive Cleavages

    I. Hydroboration (Reduction Only)

    J. Other Reductions

    K. Reviews

IV. Synthesis of Heterocyclics

A. Aziridines

B. Furans

C. Imidazoles

D. Indoles

E. Lactams

F. Lactones

G. Pyrazoles and Pyrazolines

. Pyrimidines

I. Pyridines

J. Pyrroles and Pyrrolines

K. Quinolines and Isoquinolines

L. Thiophenes

M. Other Heterocycles with One Heteroatom

N. Other Heterocycles

O. Reviews2

V. Protecting Groups

A. Hydroxyl Protecting Groups

B. Amine Protecting Groups

C. Sulfhydryl Protecting Groups

D. Terminal Acetylene Protecting Groups

E. Carboxyl Protecting Groups

F. Ketone, Aldehyde Protecting Groups

G. C=C Protecting Groups

H. Phosphate Protecting Groups

I. Sulfone Protecting Groups

VI. Useful Synthetic Preparations

A. Functional Group Preparations

1. Acids

2. Alcohols (See Also: Reduction of Carbonyls 203)

3. Alkyl Halides

4. Amides

5. Amines (See Also: Amide Reduction 208, Nitrile Reduction 208)

6. Amino Acids

7. Anhydrides

8. Arynes

9. Azides

10. Carbodiimides

11. Diazoalkanes

12. a-Diketones (See Also: Oxidative Addition to C=C 189)

13. Disulfides

14. Enamines

15. Epoxides (See Also: Oxidative Addition to C=C 189)

16. Esters

17. Isocyanates

18. Isocyanides

19. Ketals (See Also: Ketone, Aldehyde Protecting Groups 253)

20. Ketones and Aldehydes (See Also: C-O Oxidations 178)

21. ß-Dicarbonyl Compounds

22. Nitriles

23. Nitro Compounds

24. Nucleotides (See Also: Hydroxyl and Phosphate Protecting Groups 248, 254)

25. Peptides (See Also: Hydroxyl and Amine Protecting Groups 248, 250)

26. Peracids

27. Phenols (See Also: Hydroxylation of Aromatic Rings 198)

28. Phosphates

29. Sulfides

30. Vinyl Halides, Vinyl Ethers, and Vinyl Esters

    B. Multi-Step Synthetic Transformations

31. Ketone Transposition

32. Ring Enlargement

33. Other

VII. Miscellaneous Reviews

VIII. Other Completely Miscellaneous Reactions