Annual Reports in Organic Synthesis — 1985

PrefaceJournals AbstractedGlossary of AbbreviationsI. Carbon-Carbon Bond Forming Reactions A. Carbon-Carbon Single Bonds (see also: I.E, I.F, I.G) 1. Alkylation of Aldehydes, Ketones, and Their Derivatives 2. Alkylation of Nitriles, Acids, and Acid Derivatives 3. Alkylation of β-Dicarbonyl and β-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) 1. Wittig-Type Olefination Reactions 2. Eliminations 3. Other Carbon-Carbon Double Bond 4. Allene Forming Reactions C. Carbon-Carbon Triple Bonds D. Cyclopropanations 1. Carbene or Carbenoid Additions 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 3. Other Aromatic Substitutions G. Synthesis via Organometallics 1. Organoboranes 2. Carbonylation Reactions 3. Other Syntheses via Organometallics 4. ReviewsII. 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. Dehydrogenation J. Other Oxidations and ReviewsIII. Reductions A. C=0 Reductions (see also: III.F.1) B. C-N Multiple Bond Reductions 1. Nitrile Reductions 2. Imine 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 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. Reduction of Azides J. Hydroboration (reduction only) K. Other Reductions and ReviewsIV. Synthesis of Heterocycles A. Oxiranes B. Furans, Thiophenes, 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 2 Os 3. Heterocycles with 1 N and 1 O 4. Heterocycles with 1 N and 1 S 5. Heterocycles with 1 N and 1 P 6. Heterocycles with 1 S and 1 O 7. Heterocycles with 3 Ns 8. Other Heterocycles J. General ReviewsV. 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. Miscellaneous Protecting GroupsVI. Useful Synthetic Preparations A. Functional Group Preparations 1. Acids, Acid Halides, etc. (see also: II.A.2) 2. Alcohols, Phenols (see also: II.B.1, III.A, III.F.1) 3. Alkyl, Aryl Halides (see also: II.B.2) 4. Amides, etc. (see also: IV.D, VI.A.14) 5. Amines and Carbamates (see also: III.D) 6. Amino Acids and Derivatives (see also: VI.A.4) 7. Esters (see also: IV.E, V.D.) 8. Ethers (see also: V.E.) 9. Aldehydes and Ketones (see also: I.A.1, II.A.1, III.F.1) 10. Imines 11. Other N-Containing Functional Groups 12. Nucleotides, etc. 13. Phosphates 14. Peptides (see also: V.B, V.C, V.D, VI.A.4) 15. Iodonium Compounds 16. Sulfur Compounds (see also: II.E, III.C) 17. Selenium Compounds 18. Ring Enlargement 19. Ring ContractionVII. Other Reviews A. Techniques B. Asymmetric Synthesis C. Reactions D. Reactive Intermediates E. Organo-Metallics and -Metalloids F. Fluoro-Compounds and Fluorination G. Natural Products H. OthersAuthor Index