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Science of Synthesis Knowledge Updates.
The Science of Synthesis Editorial Board, together with the volume editors and authors, is constantly reviewing the whole field of synthetic organic chemistry as presented in Science of Synthesis and evaluating significant developments in synthetic methodology. Several annual volumes updating conten...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Otros Autores: | , , , , , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
NEW YORK :
Thieme,
2016.
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| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Science of Synthesis: Knowledge Updates 2016/2; Title Page; Copyright; Preface; Abstracts; Science of Synthesis Knowledge Updates 2016/2; Table of Contents; 1.2.7 Radical-Based Palladium-Catalyzed Bond Constructions; 1.2.7.1 Method 1: Reactions Involving Palladium(I) Species; 1.2.7.1.1 Variation 1: Synthesis of Organometallic Palladium(I) Complexes; 1.2.7.1.2 Variation 2: Reactions Involving Palladium(I) Precatalysts; 1.2.7.1.3 Variation 3: Cross-Coupling Reactions; 1.2.7.1.4 Variation 4: Carbonylation Reactions; 1.2.7.1.5 Variation 5: Cyclization Reactions.
- 1.2.7.1.6 Variation 6: Atom-Transfer Reactions1.2.7.2 Method 2: Reactions Involving Palladium(III) Species; 1.2.7.2.1 Variation 1: Synthesis of Organometallic Palladium(III) Complexes; 1.2.7.2.2 Variation 2: C-H Activation Reactions Involving Palladium(III); 1.2.7.2.3 Variation 3: C-F Bond-Constructing Reactions Involving Palladium(III); 1.2.7.2.4 Variation 4: Reactions Involving Phenyl or Benzoyl Radicals; 1.2.7.2.5 Variation 5: Asymmetric Aza-Claisen Rearrangements; 1.2.7.3 Method 3: Reactions Involving Palladium(I) and Palladium(III) Species; 1.2.7.4 Method 4: Miscellaneous Reactions.
- 2.11.15 C(sp3)-H Functionalization by Allylic C-H Activation of Zirconocene Complexes2.11.15.1 Method 1: Synthesis of Conjugated Dienes from Nonconjugated Dienes; 2.11.15.1.1 Variation 1: From Nonheteroatom-Substituted Alkenes; 2.11.15.1.2 Variation 2: From Nonconjugated Dienes Bearing an Alkoxy Substituent; 2.11.15.2 Method 2: Synthesis of Trienes; 2.11.15.3 Method 3: Synthesis of Homoallylic Alcohols; 2.11.15.3.1 Variation 1: From Acid Chlorides without Ligand Exchange; 2.11.15.3.2 Variation 2: From Acid Chlorides with Ligand Exchange.
- 2.11.15.3.3 Variation 3: From Aldehydes without Ligand Exchange2.11.15.3.4 Variation 4: From Aldehydes with Ligand Exchange; 2.11.15.4 Method 4: Diastereoselective Synthesis of Homoallylic Amines; 2.11.15.5 Method 5: Diastereoselective Synthesis of 1,4-Homoallylic Diols; 2.11.15.5.1 Variation 1: From Grignard Reagents; 2.11.15.5.2 Variation 2: From Terminal Alkenes; 2.11.15.6 Method 6: Synthesis of 1,2-Disubstituted Cyclopropanols; 2.11.15.7 Method 7: Synthesis of Substituted Allylic Derivatives from Unsaturated Fatty Alcohols.