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Cinchona alkaloids in synthesis and catalysis [[electronic resource] ] : ligands, immobilization and organocatalysis / / edited by Choong Eui Song
| Cinchona alkaloids in synthesis and catalysis [[electronic resource] ] : ligands, immobilization and organocatalysis / / edited by Choong Eui Song |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (547 p.) |
| Disciplina |
547.215
547.7 |
| Altri autori (Persone) | SongChoong Eui |
| Soggetto topico |
Cinchona alkaloids
Chirality Organic compounds - Synthesis Catalysis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-30251-5
9786612302510 3-527-62817-7 3-527-62818-5 |
| Classificazione |
VK 5500
VK 8620 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis; Contents; Preface; Biography; List of Contributors; 1 An Overview of Cinchona Alkaloids in Chemistry; 1.1 Brief History; 1.2 Active Sites in Cinchona Alkaloids and Their Derivatives; 1.3 Structural Information on Cinchona Alkaloids; 1.4 How This Book Is Organized; References; Part One: Cinchona Alkaloid Derivatives as Chirality Inducers in Metal-Catalyzed Reactions; 2 Cinchona Alkaloids as Chirality Transmitters in Metal-Catalyzed Asymmetric Reductions; 2.1 Introduction
2.2 Homogeneous Systems for Ketone Reductions2.3 Heterogeneous Pt and Pd Catalysts Modified with Cinchona Alkaloids; 2.3.1 Background; 2.3.2 Catalysts; 2.3.3 Modifiers and Solvents; 2.3.4 Substrate Scope for Pt Catalysts; 2.3.4.1 α-Keto Acid Derivatives; 2.3.4.2 α,γ-Diketo Esters; 2.3.4.3 Fluorinated Ketones; 2.3.4.4 α-Keto Acetals; 2.3.4.5 α-Keto Ethers; 2.3.4.6 Miscellaneous Ketones; 2.3.5 Substrate Scope for Pd Catalysts; 2.4 Industrial Applications; 2.5 Conclusions; References; 3 Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations; 3.1 Introduction 3.2 Asymmetric Dihydroxylation of Alkenes3.2.1 Early Reactions; 3.2.2 Bisalkaloid Ligands; 3.2.3 Mechanism; 3.2.4 Variations; 3.2.5 Substrates and Selectivity; 3.2.5.1 Simple Alkenes; 3.2.5.2 Functionalized Alkenes; 3.2.5.3 Polyenes; 3.2.5.3.1 Nonconjugate Olefins; 3.2.5.3.2 Conjugated Polyenes; 3.2.5.4 Double Asymmetric Induction; 3.2.5.5 Resolutions; 3.2.6 Some Reactions of 1,2-Diols; 3.2.6.1 Cyclic Sulfates and Sulfites; 3.3 Aminohydroxylation; 3.4 Sulfur Oxidations; 3.5 Summary; References 4 Cinchona Alkaloids and their Derivatives as Chirality Inducers in Metal-Promoted Enantioselective Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions4.1 Introduction; 4.2 Nucleophilic Addition to Carbonyl or Imine Compounds; 4.2.1 Organozinc Addition; 4.2.1.1 Dialkylzinc Addition to Aldehydes; 4.2.1.2 Dialkylzinc Addition to Imines; 4.2.1.3 Addition of Alkynylzincs to Carbonyls; 4.2.2 Asymmetric Reformatsky Reaction; 4.2.3 Indium-Mediated Addition; 4.2.4 Asymmetric Cyanation; 4.2.4.1 Cyanohydrin Synthesis; 4.2.4.2 Strecker Synthesis 4.2.5 Reactions of Chiral Ammonium Ketene Enolates as Nucleophiles with Different Electrophiles4.2.5.1 Lewis Acid Assisted Nucleophilic Addition of Ketenes (or Sulfenes) to Aldehydes: β-Lactone and β-Sultone Synthesis; 4.2.5.2 Lewis Acid Assisted Nucleophilic Addition of Ketenes to Imines: β-Lactam Synthesis; 4.2.5.3 Applications of Chiral Ketene Enolates to Formal [4 + 2] type Cyclization; 4.2.6 Aza-Henry Reaction; 4.2.7 Enantioselective Hydrophosphonylation; 4.3 Miscellaneous Reactions; 4.3.1 Claisen Rearrangements; 4.3.2 Pd-Catalyzed Asymmetric Allylic Substitutions 4.3.3 Pauson-Khand Reaction |
| Record Nr. | UNINA-9910139907903321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cinchona alkaloids in synthesis and catalysis [[electronic resource] ] : ligands, immobilization and organocatalysis / / edited by Choong Eui Song
| Cinchona alkaloids in synthesis and catalysis [[electronic resource] ] : ligands, immobilization and organocatalysis / / edited by Choong Eui Song |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (547 p.) |
| Disciplina |
547.215
547.7 |
| Altri autori (Persone) | SongChoong Eui |
| Soggetto topico |
Cinchona alkaloids
Chirality Organic compounds - Synthesis Catalysis |
| ISBN |
1-282-30251-5
9786612302510 3-527-62817-7 3-527-62818-5 |
| Classificazione |
VK 5500
VK 8620 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis; Contents; Preface; Biography; List of Contributors; 1 An Overview of Cinchona Alkaloids in Chemistry; 1.1 Brief History; 1.2 Active Sites in Cinchona Alkaloids and Their Derivatives; 1.3 Structural Information on Cinchona Alkaloids; 1.4 How This Book Is Organized; References; Part One: Cinchona Alkaloid Derivatives as Chirality Inducers in Metal-Catalyzed Reactions; 2 Cinchona Alkaloids as Chirality Transmitters in Metal-Catalyzed Asymmetric Reductions; 2.1 Introduction
2.2 Homogeneous Systems for Ketone Reductions2.3 Heterogeneous Pt and Pd Catalysts Modified with Cinchona Alkaloids; 2.3.1 Background; 2.3.2 Catalysts; 2.3.3 Modifiers and Solvents; 2.3.4 Substrate Scope for Pt Catalysts; 2.3.4.1 α-Keto Acid Derivatives; 2.3.4.2 α,γ-Diketo Esters; 2.3.4.3 Fluorinated Ketones; 2.3.4.4 α-Keto Acetals; 2.3.4.5 α-Keto Ethers; 2.3.4.6 Miscellaneous Ketones; 2.3.5 Substrate Scope for Pd Catalysts; 2.4 Industrial Applications; 2.5 Conclusions; References; 3 Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations; 3.1 Introduction 3.2 Asymmetric Dihydroxylation of Alkenes3.2.1 Early Reactions; 3.2.2 Bisalkaloid Ligands; 3.2.3 Mechanism; 3.2.4 Variations; 3.2.5 Substrates and Selectivity; 3.2.5.1 Simple Alkenes; 3.2.5.2 Functionalized Alkenes; 3.2.5.3 Polyenes; 3.2.5.3.1 Nonconjugate Olefins; 3.2.5.3.2 Conjugated Polyenes; 3.2.5.4 Double Asymmetric Induction; 3.2.5.5 Resolutions; 3.2.6 Some Reactions of 1,2-Diols; 3.2.6.1 Cyclic Sulfates and Sulfites; 3.3 Aminohydroxylation; 3.4 Sulfur Oxidations; 3.5 Summary; References 4 Cinchona Alkaloids and their Derivatives as Chirality Inducers in Metal-Promoted Enantioselective Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions4.1 Introduction; 4.2 Nucleophilic Addition to Carbonyl or Imine Compounds; 4.2.1 Organozinc Addition; 4.2.1.1 Dialkylzinc Addition to Aldehydes; 4.2.1.2 Dialkylzinc Addition to Imines; 4.2.1.3 Addition of Alkynylzincs to Carbonyls; 4.2.2 Asymmetric Reformatsky Reaction; 4.2.3 Indium-Mediated Addition; 4.2.4 Asymmetric Cyanation; 4.2.4.1 Cyanohydrin Synthesis; 4.2.4.2 Strecker Synthesis 4.2.5 Reactions of Chiral Ammonium Ketene Enolates as Nucleophiles with Different Electrophiles4.2.5.1 Lewis Acid Assisted Nucleophilic Addition of Ketenes (or Sulfenes) to Aldehydes: β-Lactone and β-Sultone Synthesis; 4.2.5.2 Lewis Acid Assisted Nucleophilic Addition of Ketenes to Imines: β-Lactam Synthesis; 4.2.5.3 Applications of Chiral Ketene Enolates to Formal [4 + 2] type Cyclization; 4.2.6 Aza-Henry Reaction; 4.2.7 Enantioselective Hydrophosphonylation; 4.3 Miscellaneous Reactions; 4.3.1 Claisen Rearrangements; 4.3.2 Pd-Catalyzed Asymmetric Allylic Substitutions 4.3.3 Pauson-Khand Reaction |
| Record Nr. | UNINA-9910831097003321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cinchona alkaloids in synthesis and catalysis : ligands, immobilization and organocatalysis / / edited by Choong Eui Song
| Cinchona alkaloids in synthesis and catalysis : ligands, immobilization and organocatalysis / / edited by Choong Eui Song |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (547 p.) |
| Disciplina |
547.215
547.7 |
| Altri autori (Persone) | SongChoong Eui |
| Soggetto topico |
Cinchona alkaloids
Chirality Organic compounds - Synthesis Catalysis |
| ISBN |
1-282-30251-5
9786612302510 3-527-62817-7 3-527-62818-5 |
| Classificazione |
VK 5500
VK 8620 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis; Contents; Preface; Biography; List of Contributors; 1 An Overview of Cinchona Alkaloids in Chemistry; 1.1 Brief History; 1.2 Active Sites in Cinchona Alkaloids and Their Derivatives; 1.3 Structural Information on Cinchona Alkaloids; 1.4 How This Book Is Organized; References; Part One: Cinchona Alkaloid Derivatives as Chirality Inducers in Metal-Catalyzed Reactions; 2 Cinchona Alkaloids as Chirality Transmitters in Metal-Catalyzed Asymmetric Reductions; 2.1 Introduction
2.2 Homogeneous Systems for Ketone Reductions2.3 Heterogeneous Pt and Pd Catalysts Modified with Cinchona Alkaloids; 2.3.1 Background; 2.3.2 Catalysts; 2.3.3 Modifiers and Solvents; 2.3.4 Substrate Scope for Pt Catalysts; 2.3.4.1 α-Keto Acid Derivatives; 2.3.4.2 α,γ-Diketo Esters; 2.3.4.3 Fluorinated Ketones; 2.3.4.4 α-Keto Acetals; 2.3.4.5 α-Keto Ethers; 2.3.4.6 Miscellaneous Ketones; 2.3.5 Substrate Scope for Pd Catalysts; 2.4 Industrial Applications; 2.5 Conclusions; References; 3 Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations; 3.1 Introduction 3.2 Asymmetric Dihydroxylation of Alkenes3.2.1 Early Reactions; 3.2.2 Bisalkaloid Ligands; 3.2.3 Mechanism; 3.2.4 Variations; 3.2.5 Substrates and Selectivity; 3.2.5.1 Simple Alkenes; 3.2.5.2 Functionalized Alkenes; 3.2.5.3 Polyenes; 3.2.5.3.1 Nonconjugate Olefins; 3.2.5.3.2 Conjugated Polyenes; 3.2.5.4 Double Asymmetric Induction; 3.2.5.5 Resolutions; 3.2.6 Some Reactions of 1,2-Diols; 3.2.6.1 Cyclic Sulfates and Sulfites; 3.3 Aminohydroxylation; 3.4 Sulfur Oxidations; 3.5 Summary; References 4 Cinchona Alkaloids and their Derivatives as Chirality Inducers in Metal-Promoted Enantioselective Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions4.1 Introduction; 4.2 Nucleophilic Addition to Carbonyl or Imine Compounds; 4.2.1 Organozinc Addition; 4.2.1.1 Dialkylzinc Addition to Aldehydes; 4.2.1.2 Dialkylzinc Addition to Imines; 4.2.1.3 Addition of Alkynylzincs to Carbonyls; 4.2.2 Asymmetric Reformatsky Reaction; 4.2.3 Indium-Mediated Addition; 4.2.4 Asymmetric Cyanation; 4.2.4.1 Cyanohydrin Synthesis; 4.2.4.2 Strecker Synthesis 4.2.5 Reactions of Chiral Ammonium Ketene Enolates as Nucleophiles with Different Electrophiles4.2.5.1 Lewis Acid Assisted Nucleophilic Addition of Ketenes (or Sulfenes) to Aldehydes: β-Lactone and β-Sultone Synthesis; 4.2.5.2 Lewis Acid Assisted Nucleophilic Addition of Ketenes to Imines: β-Lactam Synthesis; 4.2.5.3 Applications of Chiral Ketene Enolates to Formal [4 + 2] type Cyclization; 4.2.6 Aza-Henry Reaction; 4.2.7 Enantioselective Hydrophosphonylation; 4.3 Miscellaneous Reactions; 4.3.1 Claisen Rearrangements; 4.3.2 Pd-Catalyzed Asymmetric Allylic Substitutions 4.3.3 Pauson-Khand Reaction |
| Record Nr. | UNINA-9910877702003321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
| Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2011 |
| Descrizione fisica | 1 online resource (659 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
MajumdarKrishna C
ChattopadhyayShital K |
| Soggetto topico |
Heterocyclic compounds
Natural products - Synthesis |
| ISBN |
3-527-63489-4
1-283-37054-9 9786613370549 3-527-63490-8 3-527-63488-6 |
| Classificazione |
VK 5500
VK 7200 VK 8500 540 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems. |
| Record Nr. | UNINA-9910137853203321 |
| Weinheim, : Wiley-VCH, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
| Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2011 |
| Descrizione fisica | 1 online resource (659 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
MajumdarKrishna C
ChattopadhyayShital K |
| Soggetto topico |
Heterocyclic compounds
Natural products - Synthesis |
| ISBN |
3-527-63489-4
1-283-37054-9 9786613370549 3-527-63490-8 3-527-63488-6 |
| Classificazione |
VK 5500
VK 7200 VK 8500 540 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems. |
| Record Nr. | UNINA-9910830690903321 |
| Weinheim, : Wiley-VCH, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
| Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2011 |
| Descrizione fisica | 1 online resource (659 p.) |
| Disciplina |
547.59
547/.59 |
| Altri autori (Persone) |
MajumdarKrishna C
ChattopadhyayShital K |
| Soggetto topico |
Heterocyclic compounds
Natural products - Synthesis |
| ISBN |
3-527-63489-4
1-283-37054-9 9786613370549 3-527-63490-8 3-527-63488-6 |
| Classificazione |
VK 5500
VK 7200 VK 8500 540 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems. |
| Record Nr. | UNINA-9910877349303321 |
| Weinheim, : Wiley-VCH, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Hydroformylation for Organic Synthesis / / edited by Maurizio Taddei, André Mann
| Hydroformylation for Organic Synthesis / / edited by Maurizio Taddei, André Mann |
| Edizione | [1st ed. 2013.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 |
| Descrizione fisica | 1 online resource (VII, 229 p. 272 illus., 12 illus. in color.) |
| Disciplina | 547.1393 |
| Collana | Topics in Current Chemistry |
| Soggetto topico |
Organic chemistry
Catalysis Chemical engineering Organic Chemistry Industrial Chemistry/Chemical Engineering |
| ISBN | 3-642-45059-8 |
| Classificazione |
540
VA 1110 VK 5500 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | The role of metals and ligands in organic hydroformylation -- Hydroformylation in aqueous biphasic media assisted by molecular receptors -- Asymmetric hydroformylation -- Domino reactions triggered by hydroformylation -- Rhodium-catalyzed hydroformylation in fused azapolycycles synthesis -- Hydroformylation in natural product synthesis. |
| Record Nr. | UNINA-9910437803103321 |
| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis [[electronic resource] ] : state of the art 2005-2007 / / Douglass F. Taber
| Organic synthesis [[electronic resource] ] : state of the art 2005-2007 / / Douglass F. Taber |
| Autore | Taber D. F (Douglass F.), <1948-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, c2008 |
| Descrizione fisica | 1 online resource (242 p.) |
| Disciplina | 547.2 |
| Collana | Organic Synthesis: State of the Art |
| Soggetto topico |
Organic compounds - Synthesis
Organic compounds - Synthesis - Research |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-76689-5
9786611766894 0-470-38597-9 0-470-38596-0 |
| Classificazione |
CHE 620f
VK 5500 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Synthesis: State of the Art 2005-2007; Contents; Preface; 1. Synthesis of (-)- Littoralisone; 2. Enantiocontrolled Construction of Oxygenated and Animated Stereogenic Centers; 3. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 4. Catalytic Enantioselective Aldol/Mannich Reactions Leading to Extended Arrays of Stereogenic Centers; 5. Alternative Strategies for the Construction of Extended Arrays of Stereogenic Centers; 6. Synthesis of(-)- Avrainvillamide and (+)- Stephacidin B; 7. Best Synthetic Methods: Oxidation; 8. Best Synthetic Methods: Reduction
9. Selective Reactions of Alkenes10. Synthesis of the Potent FBBP12 Ligand Antascomicin B; 11. Best Synthetic Methods: Carbon-Carbon Bond Formation; 12. Enantioselective Construction of Quaternary Centers; 13. Pd-Mediated Arylation of Aromatic and Hetero Aromatic Rings; 14. The Overman Route to Gelsemine; 15. Stereoselective Construction of Oxygen Heterocycles; 16. Enantioselective Construction of Naturally-Occurring Cyclic Ethers; 17. Stereoselective Construction of Nitrogen Heterocycles; 18. The Stork Synthesis of (-)- Reserpine 19. Stereocontrolled Construction of Azacyclic Natural Products20. Preparation of Benzene Derivatives; 21. Preparation of Heteroaromatics; 22. Preparation and Reactions of Carboxylic Acids, Esters and Amides; 23. The Boger Route to (-)-Vindoline; 24. Protection of C-O and C-N; 25. New Catalysts and Strategies for Alkene Metathesis; 26. Creative Applications of Alkene and Alkyne Metathesis in Total Synthesis: (+)-8-epi-Xanthatin, (+)-Longicin, Latrunculin A, and Garsubellin A; 27. Synthesis of Erythronolide A; 28. Best Synthetic Methods: C-C Bond Formation 29. Catalytic Enantioselective Homologation of Aldehydes to Alcohols and Amines30. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 31. Enantioselective Construction of Arrays of Stereogenic Centers; 32. Adventures in Complex Indole Synthesis: (-)-Fischerindole I, (+)-Fischerindole G and (+)-Weltwitindolinone A; 33. New Dienes and Dienophiles for Intermolecular and Intramolecular Diels-Alder Cycloaddtions; 34. Organocatalytic Preparation of Enantiomerically-Pure Carbocycles; 35. Carbocycle Construction by the Opening of Strained Rings: Synthesis of Tremulenolide A 36. The Corey Route to the Dolabellanes: Isoedunol and β-Araneosene37. Transition-Metal Catalyzed Enantioselective Ring Construction; 38. Best Synthetic Methods: Functional Group Transformation; 39. Selective Reactions of Alkenes; 40. Synthesis and Absolute Stereochemical Assignment of (-)-Galbulimima Alkaloid 13; 41. Preparation of Benzene Derivatives; 42. Preparation of Heteroaromatic Derivatives; 43. Functional Group Transformation; 44. Functional Group Protection; 45. The Leighton Synthesis of Dolabelide D; 46. Stereocontrolled Construction of N-Heterocycles 47. Stereocontrolled Construction of O-Heterocycles |
| Record Nr. | UNINA-9910144134303321 |
Taber D. F (Douglass F.), <1948->
|
||
| Hoboken, NJ, : Wiley, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis [[electronic resource] ] : state of the art 2005-2007 / / Douglass F. Taber
| Organic synthesis [[electronic resource] ] : state of the art 2005-2007 / / Douglass F. Taber |
| Autore | Taber D. F (Douglass F.), <1948-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, c2008 |
| Descrizione fisica | 1 online resource (242 p.) |
| Disciplina | 547.2 |
| Collana | Organic Synthesis: State of the Art |
| Soggetto topico |
Organic compounds - Synthesis
Organic compounds - Synthesis - Research |
| ISBN |
1-281-76689-5
9786611766894 0-470-38597-9 0-470-38596-0 |
| Classificazione |
CHE 620f
VK 5500 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Synthesis: State of the Art 2005-2007; Contents; Preface; 1. Synthesis of (-)- Littoralisone; 2. Enantiocontrolled Construction of Oxygenated and Animated Stereogenic Centers; 3. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 4. Catalytic Enantioselective Aldol/Mannich Reactions Leading to Extended Arrays of Stereogenic Centers; 5. Alternative Strategies for the Construction of Extended Arrays of Stereogenic Centers; 6. Synthesis of(-)- Avrainvillamide and (+)- Stephacidin B; 7. Best Synthetic Methods: Oxidation; 8. Best Synthetic Methods: Reduction
9. Selective Reactions of Alkenes10. Synthesis of the Potent FBBP12 Ligand Antascomicin B; 11. Best Synthetic Methods: Carbon-Carbon Bond Formation; 12. Enantioselective Construction of Quaternary Centers; 13. Pd-Mediated Arylation of Aromatic and Hetero Aromatic Rings; 14. The Overman Route to Gelsemine; 15. Stereoselective Construction of Oxygen Heterocycles; 16. Enantioselective Construction of Naturally-Occurring Cyclic Ethers; 17. Stereoselective Construction of Nitrogen Heterocycles; 18. The Stork Synthesis of (-)- Reserpine 19. Stereocontrolled Construction of Azacyclic Natural Products20. Preparation of Benzene Derivatives; 21. Preparation of Heteroaromatics; 22. Preparation and Reactions of Carboxylic Acids, Esters and Amides; 23. The Boger Route to (-)-Vindoline; 24. Protection of C-O and C-N; 25. New Catalysts and Strategies for Alkene Metathesis; 26. Creative Applications of Alkene and Alkyne Metathesis in Total Synthesis: (+)-8-epi-Xanthatin, (+)-Longicin, Latrunculin A, and Garsubellin A; 27. Synthesis of Erythronolide A; 28. Best Synthetic Methods: C-C Bond Formation 29. Catalytic Enantioselective Homologation of Aldehydes to Alcohols and Amines30. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 31. Enantioselective Construction of Arrays of Stereogenic Centers; 32. Adventures in Complex Indole Synthesis: (-)-Fischerindole I, (+)-Fischerindole G and (+)-Weltwitindolinone A; 33. New Dienes and Dienophiles for Intermolecular and Intramolecular Diels-Alder Cycloaddtions; 34. Organocatalytic Preparation of Enantiomerically-Pure Carbocycles; 35. Carbocycle Construction by the Opening of Strained Rings: Synthesis of Tremulenolide A 36. The Corey Route to the Dolabellanes: Isoedunol and β-Araneosene37. Transition-Metal Catalyzed Enantioselective Ring Construction; 38. Best Synthetic Methods: Functional Group Transformation; 39. Selective Reactions of Alkenes; 40. Synthesis and Absolute Stereochemical Assignment of (-)-Galbulimima Alkaloid 13; 41. Preparation of Benzene Derivatives; 42. Preparation of Heteroaromatic Derivatives; 43. Functional Group Transformation; 44. Functional Group Protection; 45. The Leighton Synthesis of Dolabelide D; 46. Stereocontrolled Construction of N-Heterocycles 47. Stereocontrolled Construction of O-Heterocycles |
| Record Nr. | UNINA-9910830581303321 |
|
Taber D. F (Douglass F.), <1948->
|
||
| Hoboken, NJ, : Wiley, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis : state of the art 2005-2007 / / Douglass F. Taber
| Organic synthesis : state of the art 2005-2007 / / Douglass F. Taber |
| Autore | Taber D. F (Douglass F.), <1948-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, c2008 |
| Descrizione fisica | 1 online resource (242 p.) |
| Disciplina | 547.2 |
| Collana | Organic Synthesis: State of the Art |
| Soggetto topico |
Organic compounds - Synthesis
Organic compounds - Synthesis - Research |
| ISBN |
1-281-76689-5
9786611766894 0-470-38597-9 0-470-38596-0 |
| Classificazione |
CHE 620f
VK 5500 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Synthesis: State of the Art 2005-2007; Contents; Preface; 1. Synthesis of (-)- Littoralisone; 2. Enantiocontrolled Construction of Oxygenated and Animated Stereogenic Centers; 3. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 4. Catalytic Enantioselective Aldol/Mannich Reactions Leading to Extended Arrays of Stereogenic Centers; 5. Alternative Strategies for the Construction of Extended Arrays of Stereogenic Centers; 6. Synthesis of(-)- Avrainvillamide and (+)- Stephacidin B; 7. Best Synthetic Methods: Oxidation; 8. Best Synthetic Methods: Reduction
9. Selective Reactions of Alkenes10. Synthesis of the Potent FBBP12 Ligand Antascomicin B; 11. Best Synthetic Methods: Carbon-Carbon Bond Formation; 12. Enantioselective Construction of Quaternary Centers; 13. Pd-Mediated Arylation of Aromatic and Hetero Aromatic Rings; 14. The Overman Route to Gelsemine; 15. Stereoselective Construction of Oxygen Heterocycles; 16. Enantioselective Construction of Naturally-Occurring Cyclic Ethers; 17. Stereoselective Construction of Nitrogen Heterocycles; 18. The Stork Synthesis of (-)- Reserpine 19. Stereocontrolled Construction of Azacyclic Natural Products20. Preparation of Benzene Derivatives; 21. Preparation of Heteroaromatics; 22. Preparation and Reactions of Carboxylic Acids, Esters and Amides; 23. The Boger Route to (-)-Vindoline; 24. Protection of C-O and C-N; 25. New Catalysts and Strategies for Alkene Metathesis; 26. Creative Applications of Alkene and Alkyne Metathesis in Total Synthesis: (+)-8-epi-Xanthatin, (+)-Longicin, Latrunculin A, and Garsubellin A; 27. Synthesis of Erythronolide A; 28. Best Synthetic Methods: C-C Bond Formation 29. Catalytic Enantioselective Homologation of Aldehydes to Alcohols and Amines30. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 31. Enantioselective Construction of Arrays of Stereogenic Centers; 32. Adventures in Complex Indole Synthesis: (-)-Fischerindole I, (+)-Fischerindole G and (+)-Weltwitindolinone A; 33. New Dienes and Dienophiles for Intermolecular and Intramolecular Diels-Alder Cycloaddtions; 34. Organocatalytic Preparation of Enantiomerically-Pure Carbocycles; 35. Carbocycle Construction by the Opening of Strained Rings: Synthesis of Tremulenolide A 36. The Corey Route to the Dolabellanes: Isoedunol and β-Araneosene37. Transition-Metal Catalyzed Enantioselective Ring Construction; 38. Best Synthetic Methods: Functional Group Transformation; 39. Selective Reactions of Alkenes; 40. Synthesis and Absolute Stereochemical Assignment of (-)-Galbulimima Alkaloid 13; 41. Preparation of Benzene Derivatives; 42. Preparation of Heteroaromatic Derivatives; 43. Functional Group Transformation; 44. Functional Group Protection; 45. The Leighton Synthesis of Dolabelide D; 46. Stereocontrolled Construction of N-Heterocycles 47. Stereocontrolled Construction of O-Heterocycles |
| Record Nr. | UNINA-9910877223503321 |
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Taber D. F (Douglass F.), <1948->
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| Hoboken, NJ, : Wiley, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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