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Asymmetric synthesis with chemical and biological methods [[electronic resource] /] / edited by Dieter Enders and Karl-Erich Jaeger
| Asymmetric synthesis with chemical and biological methods [[electronic resource] /] / edited by Dieter Enders and Karl-Erich Jaeger |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
EndersDieter
JaegerKarl-Erich |
| Soggetto topico |
Asymmetric synthesis
Organic compounds - Synthesis |
| ISBN |
1-280-92158-7
9786610921584 3-527-61064-2 3-527-61063-4 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric Synthesis with Chemical and Biological Methods; Foreword; Contents; Preface; List of Contributors; 1 Stoichiometric Asymmetric Synthesis; 1.1 Development of Novel Enantioselective Synthetic Methods; 1.1.1 Introduction; 1.1.2 α-Silyl Ketone-Controlled Asymmetric Syntheses; 1.1.2.1 Regio- and Enantioselective α-Fluorination of Ketones; 1.1.2.2 α-Silyl Controlled Asymmetric Mannich Reactions; 1.1.3 Asymmetric Hetero-Michael Additions; 1.1.3.1 Asymmetric Aza-Michael Additions; 1.1.3.2 Asymmetric Oxa-Michael Additions; 1.1.3.3 Asymmetric Phospha-Michael Additions
1.1.4 Asymmetric Syntheses with Lithiated α-Aminonitriles1.1.4.1 Asymmetric Nucleophilic α-Aminoacylation; 1.1.4.2 Asymmetric Nucleophilic Alkenoylation of Aldehydes; 1.1.5 Asymmetric Electrophilic α-Substitution of Lactones and Lactams; 1.1.6 Asymmetric Synthesis of α-Phosphino Ketones and 2-Phosphino Alcohols; 1.1.7 Asymmetric Synthesis of 1,3-Diols and anti-1,3-Polyols; 1.1.8 Asymmetric Synthesis of α-Substituted Sulfonamides and Sulfonates; 1.2 Asymmetric Synthesis of Natural Products Employing the SAMP/RAMP Hydrazone Methodology; 1.2.1 Introduction; 1.2.2 Stigmatellin A 1.2.3 Callistatin A1.2.4 Dehydroiridodiol(dial) and Neonepetalactone; 1.2.5 First Enantioselective Synthesis of Dendrobatid Alkaloids Indolizidine 209I and 223J; 1.2.6 Efficient Synthesis of (2S,12 ́R)-2-(12 ́-Aminotridecyl)pyrrolidine, a Defense Alkaloid of the Mexican Bean Beetle; 1.2.7 2-epi-Deoxoprosopinine; 1.2.8 Attenol A and B; 1.2.9 Asymmetric Synthesis of (+)- and (-)-Streptenol A; 1.2.10 Sordidin; 1.2.11 Prelactone B and V; 1.3 Asymmetric Synthesis Based on Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.1 Introduction 1.3.2 Hydroxyalkylation of Sulfonimidoyl-Substituted Allylltitanium Complexes1.3.2.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.2.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.3 Aminoalkylation of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.3.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.3.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.4 Structure and Reactivity of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.4.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes 1.3.4.2 Sulfonimidoyl-Substituted Mono(allyl)titanium Complexes1.3.5 Asymmetric Synthesis of Homopropargyl Alcohols; 1.3.6 Asymmetric Synthesis of 2,3-Dihydrofurans; 1.3.7 Synthesis of Bicyclic Unsaturated Tetrahydrofurans; 1.3.8 Asymmetric Synthesis of Alkenyloxiranes; 1.3.9 Asymmetric Synthesis of Unsaturated Mono- and Bicyclic Prolines; 1.3.10 Asymmetric Synthesis of Bicyclic Amino Acids; 1.3.11 Asymmetric Synthesis of β-Amino Acids; 1.3.12 Conclusion; 1.4 The "Daniphos" Ligands: Synthesis and Catalytic Applications; 1.4.1 Introduction; 1.4.2 General Synthesis 1.4.3 Applications in Stereoselective Catalysis |
| Record Nr. | UNINA-9910144291103321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric synthesis with chemical and biological methods [[electronic resource] /] / edited by Dieter Enders and Karl-Erich Jaeger
| Asymmetric synthesis with chemical and biological methods [[electronic resource] /] / edited by Dieter Enders and Karl-Erich Jaeger |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
EndersDieter
JaegerKarl-Erich |
| Soggetto topico |
Asymmetric synthesis
Organic compounds - Synthesis |
| ISBN |
1-280-92158-7
9786610921584 3-527-61064-2 3-527-61063-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric Synthesis with Chemical and Biological Methods; Foreword; Contents; Preface; List of Contributors; 1 Stoichiometric Asymmetric Synthesis; 1.1 Development of Novel Enantioselective Synthetic Methods; 1.1.1 Introduction; 1.1.2 α-Silyl Ketone-Controlled Asymmetric Syntheses; 1.1.2.1 Regio- and Enantioselective α-Fluorination of Ketones; 1.1.2.2 α-Silyl Controlled Asymmetric Mannich Reactions; 1.1.3 Asymmetric Hetero-Michael Additions; 1.1.3.1 Asymmetric Aza-Michael Additions; 1.1.3.2 Asymmetric Oxa-Michael Additions; 1.1.3.3 Asymmetric Phospha-Michael Additions
1.1.4 Asymmetric Syntheses with Lithiated α-Aminonitriles1.1.4.1 Asymmetric Nucleophilic α-Aminoacylation; 1.1.4.2 Asymmetric Nucleophilic Alkenoylation of Aldehydes; 1.1.5 Asymmetric Electrophilic α-Substitution of Lactones and Lactams; 1.1.6 Asymmetric Synthesis of α-Phosphino Ketones and 2-Phosphino Alcohols; 1.1.7 Asymmetric Synthesis of 1,3-Diols and anti-1,3-Polyols; 1.1.8 Asymmetric Synthesis of α-Substituted Sulfonamides and Sulfonates; 1.2 Asymmetric Synthesis of Natural Products Employing the SAMP/RAMP Hydrazone Methodology; 1.2.1 Introduction; 1.2.2 Stigmatellin A 1.2.3 Callistatin A1.2.4 Dehydroiridodiol(dial) and Neonepetalactone; 1.2.5 First Enantioselective Synthesis of Dendrobatid Alkaloids Indolizidine 209I and 223J; 1.2.6 Efficient Synthesis of (2S,12 ́R)-2-(12 ́-Aminotridecyl)pyrrolidine, a Defense Alkaloid of the Mexican Bean Beetle; 1.2.7 2-epi-Deoxoprosopinine; 1.2.8 Attenol A and B; 1.2.9 Asymmetric Synthesis of (+)- and (-)-Streptenol A; 1.2.10 Sordidin; 1.2.11 Prelactone B and V; 1.3 Asymmetric Synthesis Based on Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.1 Introduction 1.3.2 Hydroxyalkylation of Sulfonimidoyl-Substituted Allylltitanium Complexes1.3.2.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.2.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.3 Aminoalkylation of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.3.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.3.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.4 Structure and Reactivity of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.4.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes 1.3.4.2 Sulfonimidoyl-Substituted Mono(allyl)titanium Complexes1.3.5 Asymmetric Synthesis of Homopropargyl Alcohols; 1.3.6 Asymmetric Synthesis of 2,3-Dihydrofurans; 1.3.7 Synthesis of Bicyclic Unsaturated Tetrahydrofurans; 1.3.8 Asymmetric Synthesis of Alkenyloxiranes; 1.3.9 Asymmetric Synthesis of Unsaturated Mono- and Bicyclic Prolines; 1.3.10 Asymmetric Synthesis of Bicyclic Amino Acids; 1.3.11 Asymmetric Synthesis of β-Amino Acids; 1.3.12 Conclusion; 1.4 The "Daniphos" Ligands: Synthesis and Catalytic Applications; 1.4.1 Introduction; 1.4.2 General Synthesis 1.4.3 Applications in Stereoselective Catalysis |
| Record Nr. | UNINA-9910830258403321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric synthesis with chemical and biological methods / / edited by Dieter Enders and Karl-Erich Jaeger
| Asymmetric synthesis with chemical and biological methods / / edited by Dieter Enders and Karl-Erich Jaeger |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
EndersDieter
JaegerKarl-Erich |
| Soggetto topico |
Asymmetric synthesis
Organic compounds - Synthesis |
| ISBN |
1-280-92158-7
9786610921584 3-527-61064-2 3-527-61063-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric Synthesis with Chemical and Biological Methods; Foreword; Contents; Preface; List of Contributors; 1 Stoichiometric Asymmetric Synthesis; 1.1 Development of Novel Enantioselective Synthetic Methods; 1.1.1 Introduction; 1.1.2 α-Silyl Ketone-Controlled Asymmetric Syntheses; 1.1.2.1 Regio- and Enantioselective α-Fluorination of Ketones; 1.1.2.2 α-Silyl Controlled Asymmetric Mannich Reactions; 1.1.3 Asymmetric Hetero-Michael Additions; 1.1.3.1 Asymmetric Aza-Michael Additions; 1.1.3.2 Asymmetric Oxa-Michael Additions; 1.1.3.3 Asymmetric Phospha-Michael Additions
1.1.4 Asymmetric Syntheses with Lithiated α-Aminonitriles1.1.4.1 Asymmetric Nucleophilic α-Aminoacylation; 1.1.4.2 Asymmetric Nucleophilic Alkenoylation of Aldehydes; 1.1.5 Asymmetric Electrophilic α-Substitution of Lactones and Lactams; 1.1.6 Asymmetric Synthesis of α-Phosphino Ketones and 2-Phosphino Alcohols; 1.1.7 Asymmetric Synthesis of 1,3-Diols and anti-1,3-Polyols; 1.1.8 Asymmetric Synthesis of α-Substituted Sulfonamides and Sulfonates; 1.2 Asymmetric Synthesis of Natural Products Employing the SAMP/RAMP Hydrazone Methodology; 1.2.1 Introduction; 1.2.2 Stigmatellin A 1.2.3 Callistatin A1.2.4 Dehydroiridodiol(dial) and Neonepetalactone; 1.2.5 First Enantioselective Synthesis of Dendrobatid Alkaloids Indolizidine 209I and 223J; 1.2.6 Efficient Synthesis of (2S,12 ́R)-2-(12 ́-Aminotridecyl)pyrrolidine, a Defense Alkaloid of the Mexican Bean Beetle; 1.2.7 2-epi-Deoxoprosopinine; 1.2.8 Attenol A and B; 1.2.9 Asymmetric Synthesis of (+)- and (-)-Streptenol A; 1.2.10 Sordidin; 1.2.11 Prelactone B and V; 1.3 Asymmetric Synthesis Based on Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.1 Introduction 1.3.2 Hydroxyalkylation of Sulfonimidoyl-Substituted Allylltitanium Complexes1.3.2.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.2.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.3 Aminoalkylation of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.3.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.3.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.4 Structure and Reactivity of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.4.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes 1.3.4.2 Sulfonimidoyl-Substituted Mono(allyl)titanium Complexes1.3.5 Asymmetric Synthesis of Homopropargyl Alcohols; 1.3.6 Asymmetric Synthesis of 2,3-Dihydrofurans; 1.3.7 Synthesis of Bicyclic Unsaturated Tetrahydrofurans; 1.3.8 Asymmetric Synthesis of Alkenyloxiranes; 1.3.9 Asymmetric Synthesis of Unsaturated Mono- and Bicyclic Prolines; 1.3.10 Asymmetric Synthesis of Bicyclic Amino Acids; 1.3.11 Asymmetric Synthesis of β-Amino Acids; 1.3.12 Conclusion; 1.4 The "Daniphos" Ligands: Synthesis and Catalytic Applications; 1.4.1 Introduction; 1.4.2 General Synthesis 1.4.3 Applications in Stereoselective Catalysis |
| Record Nr. | UNINA-9910840659703321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Stereoselective multiple bond-forming transformations in organic synthesis / / edited by Jean Rodriguez and Damien Bonne ; foreword by Dieter Enders ; contributors, Muriel Amatore [and thirty-nine others]
| Stereoselective multiple bond-forming transformations in organic synthesis / / edited by Jean Rodriguez and Damien Bonne ; foreword by Dieter Enders ; contributors, Muriel Amatore [and thirty-nine others] |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Soggetto topico |
Organic compounds - Synthesis
Stereochemistry Chemical reactions |
| ISBN |
1-119-00642-2
1-119-00622-8 1-119-00632-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; List of Contributors; Foreword; Preface; Chapter 1 Definitions and Classifications of MBFTs; 1.1 Introduction; 1.2 Definitions; 1.3 Conclusion and Outlook; References; Part I Stereoselective Synthesis of Heterocycles; Chapter 2 Five-Membered Heterocycles; 2.1 Introduction; 2.2 Monocyclic Targets; 2.2.1 1,3-Dipolar Cycloaddition; 2.2.2 Michael Addition-Initiated Domino Process; 2.2.3 Multicomponent Reactions; 2.2.4 Carbohalogenation Reactions; 2.2.5 Radical Processes; 2.3 Fused Polycyclic Targets; 2.3.1 Cycloaddition Reactions
2.3.2 Domino Cyclization Reactions 2.4 Bridged Polycyclic Targets; 2.5 Conclusion and Outlook; References; Chapter 3 Six-Membered Heterocycles; 3.1 Introduction; 3.2 Monocyclic Targets; 3.2.1 Nitrogen-Only Heterocycles; 3.2.2 Oxygen-Containing Heterocycles; 3.3 Fused Polycyclic Targets; 3.3.1 Nitrogen-Only Fused Polycyclic Targets; 3.3.2 Oxygen-Containing Fused Polycyclic Targets; 3.3.3 Sulfur-Containing Fused Polycyclic Targets; 3.4 Bridged Polycyclic Targets; 3.4.1 General Procedure for the Preparation of 2,6-DABCO-Derived Compounds 138; 3.5 Polycyclic Spiro Targets; 3.6 Summary and Outlook References Chapter 4 Other Heterocycles; 4.1 Introduction; 4.2 Synthesis of Medium-Sized Monocyclic, Fused and Bridged Polycyclic Heterocycles; 4.2.1 Ring Synthesis by Ring Transformation via Rearrangements/Ring Expansions; 4.2.2 Ring Synthesis by Annulation; 4.3 Summary and Outlook; References; Part II Stereoselective Synthesis of Carbocycles; Chapter 5 Three- and Four-Membered Carbocycles; 5.1 Introduction; 5.2 Cyclopropane Derivatives; 5.2.1 Organocatalysis and Related Reactions [Michael-Initiated Ring-Closure (MIRC) Reactions]; 5.2.2 Organometallics and Metal Catalysis 5.2.3 Lewis Acid-Promoted Sequences 5.2.4 Pericyclic Domino Strategies; 5.2.5 Radical Domino Strategies; 5.3 Cyclobutane Derivatives; 5.3.1 Organocatalyzed Cyclobutanations; 5.3.2 Organometallics and Metal Catalysis; 5.3.3 Acid- or Base-Promoted Transformations; 5.3.4 Multicomponent Reactions (MCRs); 5.4 Summary and Outlook; References; Chapter 6 Five-Membered Carbocycles; 6.1 Introduction; 6.2 Monocyclic Targets; 6.2.1 Metal-Catalyzed Reactions; 6.2.2 Organocatalytic Reactions; 6.2.3 Miscellaneous Reactions; 6.3 Fused Polycyclic Targets; 6.3.1 Metal-Catalyzed Reactions 6.3.2 Organocatalytic Reactions 6.3.3 Lewis Acid-Catalyzed Reactions; 6.3.4 Miscellaneous Reactions; 6.4 Bridged Polycyclic Targets; 6.5 Conclusion and Outlook; References; Chapter 7 Stereoselective Synthesis of Six-Membered Carbocycles; 7.1 Introduction; 7.2 Metal-Catalyzed Stereoselective Multiple Bond-Forming Transformations; 7.2.1 Introduction; 7.2.2 Cycloadditions; 7.2.3 Metal-Catalyzed Cascades as Formal [2+2+2] Cycloadditions; 7.2.4 Metal-Catalyzed Cycloisomerization Cascades; 7.3 Enantioselective Organocatalyzed Synthesis of Six-Membered Rings 7.3.1 Organocatalyzed Miscellaneous Reactions |
| Record Nr. | UNINA-9910131282303321 |
| Hoboken, New Jersey : , : Wiley, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Stereoselective multiple bond-forming transformations in organic synthesis / / edited by Jean Rodriguez and Damien Bonne ; foreword by Dieter Enders ; contributors, Muriel Amatore [and thirty-nine others]
| Stereoselective multiple bond-forming transformations in organic synthesis / / edited by Jean Rodriguez and Damien Bonne ; foreword by Dieter Enders ; contributors, Muriel Amatore [and thirty-nine others] |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley, , 2015 |
| Descrizione fisica | 1 online resource (472 p.) |
| Disciplina | 547.2 |
| Soggetto topico |
Organic compounds - Synthesis
Stereochemistry Chemical reactions |
| ISBN |
1-119-00642-2
1-119-00622-8 1-119-00632-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; List of Contributors; Foreword; Preface; Chapter 1 Definitions and Classifications of MBFTs; 1.1 Introduction; 1.2 Definitions; 1.3 Conclusion and Outlook; References; Part I Stereoselective Synthesis of Heterocycles; Chapter 2 Five-Membered Heterocycles; 2.1 Introduction; 2.2 Monocyclic Targets; 2.2.1 1,3-Dipolar Cycloaddition; 2.2.2 Michael Addition-Initiated Domino Process; 2.2.3 Multicomponent Reactions; 2.2.4 Carbohalogenation Reactions; 2.2.5 Radical Processes; 2.3 Fused Polycyclic Targets; 2.3.1 Cycloaddition Reactions
2.3.2 Domino Cyclization Reactions 2.4 Bridged Polycyclic Targets; 2.5 Conclusion and Outlook; References; Chapter 3 Six-Membered Heterocycles; 3.1 Introduction; 3.2 Monocyclic Targets; 3.2.1 Nitrogen-Only Heterocycles; 3.2.2 Oxygen-Containing Heterocycles; 3.3 Fused Polycyclic Targets; 3.3.1 Nitrogen-Only Fused Polycyclic Targets; 3.3.2 Oxygen-Containing Fused Polycyclic Targets; 3.3.3 Sulfur-Containing Fused Polycyclic Targets; 3.4 Bridged Polycyclic Targets; 3.4.1 General Procedure for the Preparation of 2,6-DABCO-Derived Compounds 138; 3.5 Polycyclic Spiro Targets; 3.6 Summary and Outlook References Chapter 4 Other Heterocycles; 4.1 Introduction; 4.2 Synthesis of Medium-Sized Monocyclic, Fused and Bridged Polycyclic Heterocycles; 4.2.1 Ring Synthesis by Ring Transformation via Rearrangements/Ring Expansions; 4.2.2 Ring Synthesis by Annulation; 4.3 Summary and Outlook; References; Part II Stereoselective Synthesis of Carbocycles; Chapter 5 Three- and Four-Membered Carbocycles; 5.1 Introduction; 5.2 Cyclopropane Derivatives; 5.2.1 Organocatalysis and Related Reactions [Michael-Initiated Ring-Closure (MIRC) Reactions]; 5.2.2 Organometallics and Metal Catalysis 5.2.3 Lewis Acid-Promoted Sequences 5.2.4 Pericyclic Domino Strategies; 5.2.5 Radical Domino Strategies; 5.3 Cyclobutane Derivatives; 5.3.1 Organocatalyzed Cyclobutanations; 5.3.2 Organometallics and Metal Catalysis; 5.3.3 Acid- or Base-Promoted Transformations; 5.3.4 Multicomponent Reactions (MCRs); 5.4 Summary and Outlook; References; Chapter 6 Five-Membered Carbocycles; 6.1 Introduction; 6.2 Monocyclic Targets; 6.2.1 Metal-Catalyzed Reactions; 6.2.2 Organocatalytic Reactions; 6.2.3 Miscellaneous Reactions; 6.3 Fused Polycyclic Targets; 6.3.1 Metal-Catalyzed Reactions 6.3.2 Organocatalytic Reactions 6.3.3 Lewis Acid-Catalyzed Reactions; 6.3.4 Miscellaneous Reactions; 6.4 Bridged Polycyclic Targets; 6.5 Conclusion and Outlook; References; Chapter 7 Stereoselective Synthesis of Six-Membered Carbocycles; 7.1 Introduction; 7.2 Metal-Catalyzed Stereoselective Multiple Bond-Forming Transformations; 7.2.1 Introduction; 7.2.2 Cycloadditions; 7.2.3 Metal-Catalyzed Cascades as Formal [2+2+2] Cycloadditions; 7.2.4 Metal-Catalyzed Cycloisomerization Cascades; 7.3 Enantioselective Organocatalyzed Synthesis of Six-Membered Rings 7.3.1 Organocatalyzed Miscellaneous Reactions |
| Record Nr. | UNINA-9910821673803321 |
| Hoboken, New Jersey : , : Wiley, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||