This workbook accompanies Organic Synthesis: Strategy and Control, the bestselling advanced organic chemistry textbook. The workbook provides a complete course for advanced organic chemistry students and includes a graded set of problems, solutions, and discussions to illustrate and develop the themes of each of the chapters in the textbook.
This workbook accompanies Organic Synthesis: Strategy and Control, the bestselling advanced organic chemistry textbook. The workbook provides a complete course for advanced organic chemistry students and includes a graded set of problems, solutions, and discussions to illustrate and develop the themes of each of the chapters in the textbook.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Dr Paul Wyatt, School of Chemistry, University of Bristol, Bristol Dr Wyatt is Director of Undergraduate Studies for the School of Chemistry at Bristol University and also Director of BRISTOL ChemLabS - a HEFCE Centre for Excellence in Teaching & Learning. Dr Stuart Warren, Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge Dr Warren is the author of the bestselling textbooks Organic Synthesis: The Disconnection Approach (Wiley) and Organic Synthesis (OUP)
Inhaltsangabe
Preface. A. Introduction: Selectivity. 1. Planning Organic Syntheses: Tactics, Strategy and Control. 2. Chemoselectivity. 3. Regioselectivity: Controlled Aldol Reactions. 4. Stereoselectivity: Stereoselective Aldol Reactions. 5. Alternative Strategies for Enone Synthesis. 6. Choosing a Strategy: The Synthesis of Cyclopentenones. B. Making Carbon-Carbon Bonds. 7. The Ortho Strategy for Aromatic Compounds. 8. -complexes of Metals. 9. Controlling the Michael Reaction. 10. Specific Enol Equivalents. 12. Allyl Anions. 13. Homoenolates. 14. Acyl Anion Equivalents. C. Carbon-Carbon Double Bonds. 15. Synthesis of Double Bonds of Defined Stereochemistry. 16. Vinyl Anions. 17. Electrophilic Attack on Alkenes. 18. Vinyl Cations. 19. Allyl Alcohols: Allyl Cation Equivalents (and More). D. Stereochemistry. 20. Control of Stereochemistry - Introduction. 21. Diastereoselectivity. 22. Resolution. 23. The Chiral Pool: Asymmetric Synthesis with Natural Products as Starting Materials. 24. Asymmetric Induction I: Reagent-Based Strategy. 25. Asymmetric Induction II: Asymmetric Catalysis: Formation of C-O and C-N Bonds. 26. Asymmetric Induction III: Asymmetric Catalysis: Formation of C-H and C-C Bonds. 27. Asymmetric Induction IV: Substrate-Based Strategy. 28. Kinetic Resolution. 29. Enzymes: biological Methods in Asymmetric Synthesis. 30. New Chiral Centres from Old: Enantiomerically Pure Compounds and Sophisticated Syntheses. 31. Strategy of Asymmetric Synthesis. E. Functional Group Strategy. 32. Functionalisation of Pyridine. 33. Oxidation of Aromatic Rings and of Enol(ate)s. 34. Functionality and Pericyclic Reactions: Nitrogen Heterocycles by Cycloadditions and Sigmatropic Rearrangements. 35. Synthesis and Chemistry of Azoles and other Heterocycles with Two or more Heteroatoms. 36. Tandem Organic Reactions. Index.
Section A: Introduction: Selectivity 1. Planning Organic Syntheses: Tactics, Strategy and Control 2. Chemoselectivity 3. Regioselectivity: Controlled Aldol Reactions 4. Stereoselectivity: Stereoselective Aldol Reactions 5. Alternative Strategies for Enone Synthesis 6. Choosing a Strategy: The Synthesis of Cyclopentenones
Section B: Making Carbon-Carbon Bonds 7. The Ortho Strategy for Aromatic Compounds 8. s-Complexes of Metals 9. Controlling the Michael Reaction 10. Specific Enol Equivalents 11. Extended Enolates 12. Allyl Anions 13. Homoenolates 14. Acyl Anion Equivalents
Section C: Carbon-Carbon Double Bonds 15. Synthesis of Double Bonds of Defined Stereochemistry 16. Vinyl Anions 17. Electrophilic Attack on Alkenes 18. Vinyl Cations 19. Allyl Alcohols: Allyl Cation Equivalents (and More)
Section D: Stereochemistry 20. Control of Stereochemistry -- Introduction 21. Diastereoselectivity 22. Resolution 23. The Chiral Pool: Asymmetric Synthesis with Natural Products as Starting Materials 24. Asymmetric Induction I: Reagent-Based Strategy 25. Asymmetric Induction II: Asymmetric Catalysis: Formation of C-O and C-N Bonds 26. Asymmetric Induction III: Asymmetric Catalysis: Formation of C-H and C-C Bonds 27. Asymmetric Induction IV: Substrate-Based Strategy 28. Kinetic Resolution 29. Enzymes: Biological Methods in Asymmetric Synthesis 30. New Chiral Centres from Old: Enantiomerically Pure Compounds & Sophisticated Syntheses 31. Strategy of Asymmetric Synthesis
Section E: Functional Group Strategy 32. Functionalisation of Pyridine 33. Oxidation of Aromatic Rings and of Enol(ate)s 34. Functionality and Pericyclic Reactions: Nitrogen Heterocycles by Cycloadditions and Sigmatropic Rearrangements 35. Synthesis and Chemistry of Azoles and other Heterocycles with Two or more Heteroatoms 36. Tandem Organic Reactions
Preface. A. Introduction: Selectivity. 1. Planning Organic Syntheses: Tactics, Strategy and Control. 2. Chemoselectivity. 3. Regioselectivity: Controlled Aldol Reactions. 4. Stereoselectivity: Stereoselective Aldol Reactions. 5. Alternative Strategies for Enone Synthesis. 6. Choosing a Strategy: The Synthesis of Cyclopentenones. B. Making Carbon-Carbon Bonds. 7. The Ortho Strategy for Aromatic Compounds. 8. -complexes of Metals. 9. Controlling the Michael Reaction. 10. Specific Enol Equivalents. 12. Allyl Anions. 13. Homoenolates. 14. Acyl Anion Equivalents. C. Carbon-Carbon Double Bonds. 15. Synthesis of Double Bonds of Defined Stereochemistry. 16. Vinyl Anions. 17. Electrophilic Attack on Alkenes. 18. Vinyl Cations. 19. Allyl Alcohols: Allyl Cation Equivalents (and More). D. Stereochemistry. 20. Control of Stereochemistry - Introduction. 21. Diastereoselectivity. 22. Resolution. 23. The Chiral Pool: Asymmetric Synthesis with Natural Products as Starting Materials. 24. Asymmetric Induction I: Reagent-Based Strategy. 25. Asymmetric Induction II: Asymmetric Catalysis: Formation of C-O and C-N Bonds. 26. Asymmetric Induction III: Asymmetric Catalysis: Formation of C-H and C-C Bonds. 27. Asymmetric Induction IV: Substrate-Based Strategy. 28. Kinetic Resolution. 29. Enzymes: biological Methods in Asymmetric Synthesis. 30. New Chiral Centres from Old: Enantiomerically Pure Compounds and Sophisticated Syntheses. 31. Strategy of Asymmetric Synthesis. E. Functional Group Strategy. 32. Functionalisation of Pyridine. 33. Oxidation of Aromatic Rings and of Enol(ate)s. 34. Functionality and Pericyclic Reactions: Nitrogen Heterocycles by Cycloadditions and Sigmatropic Rearrangements. 35. Synthesis and Chemistry of Azoles and other Heterocycles with Two or more Heteroatoms. 36. Tandem Organic Reactions. Index.
Section A: Introduction: Selectivity 1. Planning Organic Syntheses: Tactics, Strategy and Control 2. Chemoselectivity 3. Regioselectivity: Controlled Aldol Reactions 4. Stereoselectivity: Stereoselective Aldol Reactions 5. Alternative Strategies for Enone Synthesis 6. Choosing a Strategy: The Synthesis of Cyclopentenones
Section B: Making Carbon-Carbon Bonds 7. The Ortho Strategy for Aromatic Compounds 8. s-Complexes of Metals 9. Controlling the Michael Reaction 10. Specific Enol Equivalents 11. Extended Enolates 12. Allyl Anions 13. Homoenolates 14. Acyl Anion Equivalents
Section C: Carbon-Carbon Double Bonds 15. Synthesis of Double Bonds of Defined Stereochemistry 16. Vinyl Anions 17. Electrophilic Attack on Alkenes 18. Vinyl Cations 19. Allyl Alcohols: Allyl Cation Equivalents (and More)
Section D: Stereochemistry 20. Control of Stereochemistry -- Introduction 21. Diastereoselectivity 22. Resolution 23. The Chiral Pool: Asymmetric Synthesis with Natural Products as Starting Materials 24. Asymmetric Induction I: Reagent-Based Strategy 25. Asymmetric Induction II: Asymmetric Catalysis: Formation of C-O and C-N Bonds 26. Asymmetric Induction III: Asymmetric Catalysis: Formation of C-H and C-C Bonds 27. Asymmetric Induction IV: Substrate-Based Strategy 28. Kinetic Resolution 29. Enzymes: Biological Methods in Asymmetric Synthesis 30. New Chiral Centres from Old: Enantiomerically Pure Compounds & Sophisticated Syntheses 31. Strategy of Asymmetric Synthesis
Section E: Functional Group Strategy 32. Functionalisation of Pyridine 33. Oxidation of Aromatic Rings and of Enol(ate)s 34. Functionality and Pericyclic Reactions: Nitrogen Heterocycles by Cycloadditions and Sigmatropic Rearrangements 35. Synthesis and Chemistry of Azoles and other Heterocycles with Two or more Heteroatoms 36. Tandem Organic Reactions
Rezensionen
?This is a must-read for any final year undergrad or PhD? student in organic chemistry, but it s more than that?it s a book for experienced chemists too.? ( Reviews , May 2009)
Es gelten unsere Allgemeinen Geschäftsbedingungen: www.buecher.de/agb
Impressum
www.buecher.de ist ein Internetauftritt der buecher.de internetstores GmbH
Geschäftsführung: Monica Sawhney | Roland Kölbl | Günter Hilger
Sitz der Gesellschaft: Batheyer Straße 115 - 117, 58099 Hagen
Postanschrift: Bürgermeister-Wegele-Str. 12, 86167 Augsburg
Amtsgericht Hagen HRB 13257
Steuernummer: 321/5800/1497
USt-IdNr: DE450055826
