| Description |
1 online resource (520 pages) |
| Contents |
880-01 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 |
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880-01/(S 2.11.15.8 Method 8: Selective Reduction of the Double Bond of ω-Ene Dihydrofurans and Dihydropyrans2.11.15.9 Method 9: Synthesis of Acyclic Fragments Possessing an All-Carbon Quaternary Stereogenic Center; 2.11.15.9.1 Variation 1: From ω-Ene Cyclopropanes; 2.11.15.9.2 Variation 2: From Alkylidenecyclopropanes; 2.11.15.9.3 Variation 3: From ω-Alkenylcyclopropanes Bearing a Leaving Group; 2.11.16 Synthesis and Reactivity of Heteroatom-Substituted Vinylzirconocene Derivatives and Hetarylzirconocenes; 2.11.16.1 General Preparation of Vinylzirconocene Derivatives |
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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 |
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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 |
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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 |
| Summary |
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 content across all categories ensure that you always have access to state-of-the-art synthetic methodology |
| Notes |
2.11.16.2 General Reactivity of Vinylzirconocene Derivatives |
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Print version record |
| Subject |
Chemistry, Organic.
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Chemistry, Organic
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organic chemistry.
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Chemistry, Organic.
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| Form |
Electronic book
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| Author |
Nokami, Toshiki
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Jiang, Xuefeng
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Molander, Professor Gary A
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Schaumann, Ernst
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Shibasaki, Masakatsu
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Thomas, Eric Jim
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| ISBN |
9783132209015 |
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3132209015 |
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