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Basic concepts in organic stereochemistry / / Sunil Kumar Talapatra, Bani Talapatra
| Basic concepts in organic stereochemistry / / Sunil Kumar Talapatra, Bani Talapatra |
| Autore | Talapatra Sunil Kumar |
| Edizione | [1st ed. 2022.] |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer, , [2022] |
| Descrizione fisica | 1 online resource (266 pages) |
| Disciplina | 547.1223 |
| Soggetto topico | Stereochemistry |
| ISBN | 3-030-95990-2 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Symmetry and Molecular Chirality. Conformation, Stability, and Physical Properties -- Configurational Nomenclature. Physical Properties of Geometrical Isomers -- Projection (Fischer, Newman, Sawhorse) and Perspective (Flying Wedge and Zigzag) Formulas, Working out Stereoisomers -- Prochirality and Prostereoisomerism. Topicity of Ligands and Faces Nomenclature [1–5] -- Asymmetric Synthesis -- Some Other Aspects of Dynamic Stereochemistry: Conformation and Reactivity -- Conformation of Saturated Six-Membered Ring Compounds -- Cyclohexanone -- Fused Ring Systems -- Stereoisomerism: Axial Chirality, Planar Chirality, (R,S) Notations Helicity -- Chiroptical Properties I: Optical Rotation. ORD, CD [1-4] -- Chiroptical Properties II: Helicity Rule or Chirality Rule. |
| Record Nr. | UNINA-9910637715803321 |
Talapatra Sunil Kumar
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| Cham, Switzerland : , : Springer, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Basic organic stereochemistry / Ernest L. Eliel, Samuel H. Wilen, Michael P. Doyle
| Basic organic stereochemistry / Ernest L. Eliel, Samuel H. Wilen, Michael P. Doyle |
| Autore | Eliel, Ernest L. |
| Pubbl/distr/stampa | New York [etc.] : Wiley-Interscience, 2001 |
| Descrizione fisica | XIV, 688 p. : ill. ; 24 cm. |
| Disciplina | 547.1223 |
| Altri autori (Persone) |
Wilen, Samuel H.
Doyle, Michael F. |
| Soggetto topico |
Chimica organica
Stereochimica |
| ISBN | 978-0-471-37499-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000033630 |
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Eliel, Ernest L.
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| New York [etc.] : Wiley-Interscience, 2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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Chimica organica / Robert Thornton Morrison, Robert Neilson Boyd ; a cura di Paolo Grunanger e Paola Vita Finzi
| Chimica organica / Robert Thornton Morrison, Robert Neilson Boyd ; a cura di Paolo Grunanger e Paola Vita Finzi |
| Autore | Morrison, Robert Thornton |
| Edizione | [3. ed.] |
| Pubbl/distr/stampa | Milano : Casa Editrice Ambrosiana, c1976 |
| Descrizione fisica | VII, 1314 p. : ill. ; 25 cm. |
| Disciplina | 547.1223 |
| Altri autori (Persone) | Boyd, Robert Neilson |
| Soggetto topico | Chimica organica |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNIBAS-000006341 |
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Morrison, Robert Thornton
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| Milano : Casa Editrice Ambrosiana, c1976 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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Enantioselective chemical synthesis : methods, logic and practice / E.J. Corey and László Kürti
| Enantioselective chemical synthesis : methods, logic and practice / E.J. Corey and László Kürti |
| Autore | Corey, E. J |
| Pubbl/distr/stampa | Dallas (Texas) : Direct Book Publishing, 2010 |
| Descrizione fisica | VI, 328 p. : ill. ; 26 cm. |
| Disciplina |
547.2
547.1223 |
| Altri autori (Persone) | Kürti, László |
| Soggetto topico | Reazioni chimiche organiche - Sintesi |
| ISBN | 978-0-615-39515-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000039015 |
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Corey, E. J
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| Dallas (Texas) : Direct Book Publishing, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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Organic structural spectroscopy / Joseph B. Lambert, Herbert F. Shurvell, David A. Lightner, R. Graham Cooks
| Organic structural spectroscopy / Joseph B. Lambert, Herbert F. Shurvell, David A. Lightner, R. Graham Cooks |
| Pubbl/distr/stampa | Upper Saddle River (New Jersey) : Prentice-Hall, c1998 |
| Descrizione fisica | VIII, 568 p. : ill. ; 28 cm. |
| Disciplina |
547.122
547.1223 |
| Altri autori (Persone) |
Lambert, Joseph B.
Shurvell, Herbert F. Lightner, David A. Graham Cooks, R. |
| Soggetto topico |
Composti organici - Analisi spettroscopica
Spettroscopia |
| ISBN | 0-13-258690-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000004352 |
| Upper Saddle River (New Jersey) : Prentice-Hall, c1998 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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Quaternary stereocenters [[electronic resource] ] : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro
| Quaternary stereocenters [[electronic resource] ] : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547.1223 |
| Altri autori (Persone) |
ChristoffersJens
BaroAngelika |
| Soggetto topico |
Stereochemistry
Organic compounds - Synthesis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-85406-5
9786610854066 3-527-60685-8 3-527-60697-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Quaternary Stereocenters; Contents; Foreword; Preface; List of Contributors; Symbols and Abbreviations; 1 Important Natural Products; 1.1 Introduction; 1.2 Alkylation of Tertiary Carbon Centers; 1.3 Cycloaddition to Alkenes; 1.3.1 Diels-Alder Reaction; 1.3.2 Other Types of Cycloaddition; 1.4 Rearrangement Reactions; 1.5 Carbometallation Reactions; 1.5.1 Addition of a Carbon Nucleophile to a β,β-Disubstituted α,β-Unsaturated Enone; 1.5.2 Asymmetric and Diastereomeric Addition of a Carbon Nucleophile to Unactivated Alkenes Catalyzed by Palladium [42]; 1.6 C-H Functionalization Reactions
1.7 Asymmetric Modification of Enantiotopic/Diastereotopic Substituents of Quaternary Carbon Centers1.8 Summary; 2 Important Pharmaceuticals and Intermediates; 2.1 The Chirality of Drugs and Agrochemicals; 2.2 Steroids; 2.3 Pharmaceuticals and Agrochemicals Based on α-Dialkylated Amino Acids; 2.4 Azole Antimycotics; 2.5 Alkaloids; 2.6 HIV Inhibitors; 2.7 β-Lactam Antibiotics; 2.8 The Tetracyclines; 2.9 Summary and Outlook; 3 Aldol Reactions; 3.1 Introduction; 3.2 Metal Enolates; 3.2.1 Lithium Enolates; 3.2.2 Titanium and Zirconium Enolates; 3.2.3 Boron Enolates; 3.3 Catalytic Aldol Additions 3.3.1 Fluoride-ion-mediated Aldol Addition3.3.2 Lewis-acid-mediated Mukaiyama-type Aldol Reactions; 3.3.3 Direct Aldol Additions; 3.3.4 Organocatalysis; 3.3.5 Enzyme and Antibody Catalysis; 3.4 Conclusions; 3.5 Note Added in Proof; 4 Michael Reactions and Conjugate Additions; 4.1 Introduction; 4.2 Chiral Brönstedt Bases; 4.2.1 Cinchona Alkaloids; 4.2.2 Polymer-bound Alkaloids; 4.2.3 Organocatalysis; 4.2.4 Miscellaneous Examples; 4.3 Chiral Metal Complexes; 4.3.1 Cobalt and Copper Catalysis; 4.3.2 Rhodium Catalysis; 4.3.3 Heterobimetallic Catalysis; 4.3.4 Miscellaneous Examples 4.4 Chiral Auxiliaries4.4.1 α-Phenethylamine; 4.4.2 L-Valine Ester; 4.4.3 L-Valine Diethylamide; 4.4.4 Miscellaneous Examples; 5 Rearrangement Reactions; 5.1 Introduction; 5.2 Applications; 5.2.1 The Claisen Rearrangement; 5.2.2 The Overman Rearrangement; 5.2.3 The Cope Rearrangement; 5.2.4 The Wittig Rearrangement; 5.2.5 Semipinacol Rearrangements; 5.2.6 Miscellaneous; 5.3 Summary; 6 Cycloaddition Reactions; 6.1 Introduction; 6.2 [2+1] Cycloaddition Reactions; 6.3 [2+2] Cycloaddition Reactions; 6.4 1,3-Dipolar Cycloaddition Reactions; 6.4.1 Nitrone Cycloadditions 6.4.2 Other 1,3-Dipolar Cycloadditions6.5 Diels-Alder Reactions; 6.6 Hetero-Diels-Alder Reactions; 6.6.1 The Carbonyl Group as Dienophile; 6.6.2 α,β-Unsaturated Carbonyl Derivatives as Heterodienes; 6.6.3 Imine Derivatives as Heterodienophiles; 6.7 Consecutive Cycloaddition Reactions; 7 Asymmetric Cross-coupling and Mizoroki-Heck Reactions; 7.1 The Asymmetric Heck Reaction; 7.1.1 Introduction; 7.1.2 Mizoroki-Heck Reaction Mechanism; 7.1.3 Asymmetric Formation of Quaternary Carbon Centers; 7.2 Metal-catalyzed Cross-coupling Reactions; 7.2.1 Palladium-catalyzed α-Arylation 7.2.2 Palladium-catalyzed α-Vinylation |
| Record Nr. | UNINA-9910144324603321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Quaternary stereocenters [[electronic resource] ] : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro
| Quaternary stereocenters [[electronic resource] ] : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547.1223 |
| Altri autori (Persone) |
ChristoffersJens
BaroAngelika |
| Soggetto topico |
Stereochemistry
Organic compounds - Synthesis |
| ISBN |
1-280-85406-5
9786610854066 3-527-60685-8 3-527-60697-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Quaternary Stereocenters; Contents; Foreword; Preface; List of Contributors; Symbols and Abbreviations; 1 Important Natural Products; 1.1 Introduction; 1.2 Alkylation of Tertiary Carbon Centers; 1.3 Cycloaddition to Alkenes; 1.3.1 Diels-Alder Reaction; 1.3.2 Other Types of Cycloaddition; 1.4 Rearrangement Reactions; 1.5 Carbometallation Reactions; 1.5.1 Addition of a Carbon Nucleophile to a β,β-Disubstituted α,β-Unsaturated Enone; 1.5.2 Asymmetric and Diastereomeric Addition of a Carbon Nucleophile to Unactivated Alkenes Catalyzed by Palladium [42]; 1.6 C-H Functionalization Reactions
1.7 Asymmetric Modification of Enantiotopic/Diastereotopic Substituents of Quaternary Carbon Centers1.8 Summary; 2 Important Pharmaceuticals and Intermediates; 2.1 The Chirality of Drugs and Agrochemicals; 2.2 Steroids; 2.3 Pharmaceuticals and Agrochemicals Based on α-Dialkylated Amino Acids; 2.4 Azole Antimycotics; 2.5 Alkaloids; 2.6 HIV Inhibitors; 2.7 β-Lactam Antibiotics; 2.8 The Tetracyclines; 2.9 Summary and Outlook; 3 Aldol Reactions; 3.1 Introduction; 3.2 Metal Enolates; 3.2.1 Lithium Enolates; 3.2.2 Titanium and Zirconium Enolates; 3.2.3 Boron Enolates; 3.3 Catalytic Aldol Additions 3.3.1 Fluoride-ion-mediated Aldol Addition3.3.2 Lewis-acid-mediated Mukaiyama-type Aldol Reactions; 3.3.3 Direct Aldol Additions; 3.3.4 Organocatalysis; 3.3.5 Enzyme and Antibody Catalysis; 3.4 Conclusions; 3.5 Note Added in Proof; 4 Michael Reactions and Conjugate Additions; 4.1 Introduction; 4.2 Chiral Brönstedt Bases; 4.2.1 Cinchona Alkaloids; 4.2.2 Polymer-bound Alkaloids; 4.2.3 Organocatalysis; 4.2.4 Miscellaneous Examples; 4.3 Chiral Metal Complexes; 4.3.1 Cobalt and Copper Catalysis; 4.3.2 Rhodium Catalysis; 4.3.3 Heterobimetallic Catalysis; 4.3.4 Miscellaneous Examples 4.4 Chiral Auxiliaries4.4.1 α-Phenethylamine; 4.4.2 L-Valine Ester; 4.4.3 L-Valine Diethylamide; 4.4.4 Miscellaneous Examples; 5 Rearrangement Reactions; 5.1 Introduction; 5.2 Applications; 5.2.1 The Claisen Rearrangement; 5.2.2 The Overman Rearrangement; 5.2.3 The Cope Rearrangement; 5.2.4 The Wittig Rearrangement; 5.2.5 Semipinacol Rearrangements; 5.2.6 Miscellaneous; 5.3 Summary; 6 Cycloaddition Reactions; 6.1 Introduction; 6.2 [2+1] Cycloaddition Reactions; 6.3 [2+2] Cycloaddition Reactions; 6.4 1,3-Dipolar Cycloaddition Reactions; 6.4.1 Nitrone Cycloadditions 6.4.2 Other 1,3-Dipolar Cycloadditions6.5 Diels-Alder Reactions; 6.6 Hetero-Diels-Alder Reactions; 6.6.1 The Carbonyl Group as Dienophile; 6.6.2 α,β-Unsaturated Carbonyl Derivatives as Heterodienes; 6.6.3 Imine Derivatives as Heterodienophiles; 6.7 Consecutive Cycloaddition Reactions; 7 Asymmetric Cross-coupling and Mizoroki-Heck Reactions; 7.1 The Asymmetric Heck Reaction; 7.1.1 Introduction; 7.1.2 Mizoroki-Heck Reaction Mechanism; 7.1.3 Asymmetric Formation of Quaternary Carbon Centers; 7.2 Metal-catalyzed Cross-coupling Reactions; 7.2.1 Palladium-catalyzed α-Arylation 7.2.2 Palladium-catalyzed α-Vinylation |
| Record Nr. | UNINA-9910830617403321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Quaternary stereocenters : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro
| Quaternary stereocenters : challenges and solutions for organic synthesis / / edited by Jens Christoffers, Angelika Baro |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (362 p.) |
| Disciplina | 547.1223 |
| Altri autori (Persone) |
ChristoffersJens
BaroAngelika |
| Soggetto topico |
Stereochemistry
Organic compounds - Synthesis |
| ISBN |
1-280-85406-5
9786610854066 3-527-60685-8 3-527-60697-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Quaternary Stereocenters; Contents; Foreword; Preface; List of Contributors; Symbols and Abbreviations; 1 Important Natural Products; 1.1 Introduction; 1.2 Alkylation of Tertiary Carbon Centers; 1.3 Cycloaddition to Alkenes; 1.3.1 Diels-Alder Reaction; 1.3.2 Other Types of Cycloaddition; 1.4 Rearrangement Reactions; 1.5 Carbometallation Reactions; 1.5.1 Addition of a Carbon Nucleophile to a β,β-Disubstituted α,β-Unsaturated Enone; 1.5.2 Asymmetric and Diastereomeric Addition of a Carbon Nucleophile to Unactivated Alkenes Catalyzed by Palladium [42]; 1.6 C-H Functionalization Reactions
1.7 Asymmetric Modification of Enantiotopic/Diastereotopic Substituents of Quaternary Carbon Centers1.8 Summary; 2 Important Pharmaceuticals and Intermediates; 2.1 The Chirality of Drugs and Agrochemicals; 2.2 Steroids; 2.3 Pharmaceuticals and Agrochemicals Based on α-Dialkylated Amino Acids; 2.4 Azole Antimycotics; 2.5 Alkaloids; 2.6 HIV Inhibitors; 2.7 β-Lactam Antibiotics; 2.8 The Tetracyclines; 2.9 Summary and Outlook; 3 Aldol Reactions; 3.1 Introduction; 3.2 Metal Enolates; 3.2.1 Lithium Enolates; 3.2.2 Titanium and Zirconium Enolates; 3.2.3 Boron Enolates; 3.3 Catalytic Aldol Additions 3.3.1 Fluoride-ion-mediated Aldol Addition3.3.2 Lewis-acid-mediated Mukaiyama-type Aldol Reactions; 3.3.3 Direct Aldol Additions; 3.3.4 Organocatalysis; 3.3.5 Enzyme and Antibody Catalysis; 3.4 Conclusions; 3.5 Note Added in Proof; 4 Michael Reactions and Conjugate Additions; 4.1 Introduction; 4.2 Chiral Brönstedt Bases; 4.2.1 Cinchona Alkaloids; 4.2.2 Polymer-bound Alkaloids; 4.2.3 Organocatalysis; 4.2.4 Miscellaneous Examples; 4.3 Chiral Metal Complexes; 4.3.1 Cobalt and Copper Catalysis; 4.3.2 Rhodium Catalysis; 4.3.3 Heterobimetallic Catalysis; 4.3.4 Miscellaneous Examples 4.4 Chiral Auxiliaries4.4.1 α-Phenethylamine; 4.4.2 L-Valine Ester; 4.4.3 L-Valine Diethylamide; 4.4.4 Miscellaneous Examples; 5 Rearrangement Reactions; 5.1 Introduction; 5.2 Applications; 5.2.1 The Claisen Rearrangement; 5.2.2 The Overman Rearrangement; 5.2.3 The Cope Rearrangement; 5.2.4 The Wittig Rearrangement; 5.2.5 Semipinacol Rearrangements; 5.2.6 Miscellaneous; 5.3 Summary; 6 Cycloaddition Reactions; 6.1 Introduction; 6.2 [2+1] Cycloaddition Reactions; 6.3 [2+2] Cycloaddition Reactions; 6.4 1,3-Dipolar Cycloaddition Reactions; 6.4.1 Nitrone Cycloadditions 6.4.2 Other 1,3-Dipolar Cycloadditions6.5 Diels-Alder Reactions; 6.6 Hetero-Diels-Alder Reactions; 6.6.1 The Carbonyl Group as Dienophile; 6.6.2 α,β-Unsaturated Carbonyl Derivatives as Heterodienes; 6.6.3 Imine Derivatives as Heterodienophiles; 6.7 Consecutive Cycloaddition Reactions; 7 Asymmetric Cross-coupling and Mizoroki-Heck Reactions; 7.1 The Asymmetric Heck Reaction; 7.1.1 Introduction; 7.1.2 Mizoroki-Heck Reaction Mechanism; 7.1.3 Asymmetric Formation of Quaternary Carbon Centers; 7.2 Metal-catalyzed Cross-coupling Reactions; 7.2.1 Palladium-catalyzed α-Arylation 7.2.2 Palladium-catalyzed α-Vinylation |
| Record Nr. | UNINA-9911019927203321 |
| Weinheim, : Wiley-VCH | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Stereochemistry / David G. Morris
| Stereochemistry / David G. Morris |
| Autore | Morris, David G. |
| Pubbl/distr/stampa |
Cambridge (England) : < |
| Descrizione fisica | VII, 170 p. ; 25 cm. |
| Disciplina | 547.1223 |
| Collana | Tutorial chemistry texts |
| Soggetto topico | Stereochimica |
| ISBN | 0-85404-602-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000011889 |
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Morris, David G.
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| Cambridge (England) : <<The>> Royal Society of Chemistry, c2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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Stereochemistry of organic compounds / Ernest L. Eliel, Samuel H. Wilen ; with a chapter on stereoselective synthesis by Lewis N. Mander
| Stereochemistry of organic compounds / Ernest L. Eliel, Samuel H. Wilen ; with a chapter on stereoselective synthesis by Lewis N. Mander |
| Autore | Eliel, Ernest Ludwig |
| Pubbl/distr/stampa | New York [etc.] : Wiley-Interscience, 1994 |
| Descrizione fisica | XV, 1267 p. ; 26 cm. |
| Disciplina | 547.1223 |
| Altri autori (Persone) | Wilen, Samuel H. |
| Soggetto topico |
Stereochimica
Composti organici |
| ISBN | 978-0-471-01670-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000033763 |
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Eliel, Ernest Ludwig
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| New York [etc.] : Wiley-Interscience, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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