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Amino acids and the asymmetry of life [[electronic resource] ] : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan
| Amino acids and the asymmetry of life [[electronic resource] ] : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan |
| Autore | Meierhenrich Uwe |
| Edizione | [1st ed. 2008.] |
| Pubbl/distr/stampa | Berlin, : Springer, c2008 |
| Descrizione fisica | 1 online resource (258 p.) |
| Disciplina |
572.65
576.83 |
| Collana | Advances in astrobiology and biogeophysics |
| Soggetto topico |
Exobiology
Life - Origin Asymmetry (Chemistry) |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-86226-6
9786611862268 3-540-76886-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Tracing Life’s Origin: From Amino Acids to Space Mission ROSETTA -- Stereochemistry for the Study of the Origin of Life -- Minority Report: Life’s Chiral Molecules of Opposite Handedness -- When Crystals Deliver Chirality to Life -- When Parity Falls: The Weak Nuclear Interaction -- Chiral Fields: Light, Magnetism, and Chirality -- Key to the Prebiotic Origin of Amino Acids -- A New Record for Chiral Molecules in Meteorites -- The New Space Race: Chiral Molecules on Comets and on Mars -- Accelerating the Carousel: Amplification Mechanisms. |
| Record Nr. | UNINA-9910451495403321 |
Meierhenrich Uwe
|
||
| Berlin, : Springer, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino acids and the asymmetry of life [[electronic resource] ] : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan
| Amino acids and the asymmetry of life [[electronic resource] ] : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan |
| Autore | Meierhenrich Uwe |
| Edizione | [1st ed. 2008.] |
| Pubbl/distr/stampa | Berlin, : Springer, c2008 |
| Descrizione fisica | 1 online resource (258 p.) |
| Disciplina |
572.65
576.83 |
| Collana | Advances in astrobiology and biogeophysics |
| Soggetto topico |
Exobiology
Life - Origin Asymmetry (Chemistry) |
| ISBN |
1-281-86226-6
9786611862268 3-540-76886-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Tracing Life’s Origin: From Amino Acids to Space Mission ROSETTA -- Stereochemistry for the Study of the Origin of Life -- Minority Report: Life’s Chiral Molecules of Opposite Handedness -- When Crystals Deliver Chirality to Life -- When Parity Falls: The Weak Nuclear Interaction -- Chiral Fields: Light, Magnetism, and Chirality -- Key to the Prebiotic Origin of Amino Acids -- A New Record for Chiral Molecules in Meteorites -- The New Space Race: Chiral Molecules on Comets and on Mars -- Accelerating the Carousel: Amplification Mechanisms. |
| Record Nr. | UNINA-9910782092303321 |
|
Meierhenrich Uwe
|
||
| Berlin, : Springer, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino acids and the asymmetry of life : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan
| Amino acids and the asymmetry of life : caught in the act of formation / / Uwe Meierhenrich ; with a foreword by Henri B. Kagan |
| Autore | Meierhenrich Uwe |
| Edizione | [1st ed. 2008.] |
| Pubbl/distr/stampa | Berlin, : Springer, c2008 |
| Descrizione fisica | 1 online resource (258 p.) |
| Disciplina |
572.65
576.83 |
| Collana | Advances in astrobiology and biogeophysics |
| Soggetto topico |
Exobiology
Life - Origin Asymmetry (Chemistry) |
| ISBN |
1-281-86226-6
9786611862268 3-540-76886-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Tracing Life’s Origin: From Amino Acids to Space Mission ROSETTA -- Stereochemistry for the Study of the Origin of Life -- Minority Report: Life’s Chiral Molecules of Opposite Handedness -- When Crystals Deliver Chirality to Life -- When Parity Falls: The Weak Nuclear Interaction -- Chiral Fields: Light, Magnetism, and Chirality -- Key to the Prebiotic Origin of Amino Acids -- A New Record for Chiral Molecules in Meteorites -- The New Space Race: Chiral Molecules on Comets and on Mars -- Accelerating the Carousel: Amplification Mechanisms. |
| Record Nr. | UNINA-9910824395503321 |
|
Meierhenrich Uwe
|
||
| Berlin, : Springer, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric phase transfer catalysis / / edited by Keiji Maruoka
| Asymmetric phase transfer catalysis / / edited by Keiji Maruoka |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 |
| Descrizione fisica | 1 online resource (230 p.) |
| Disciplina | 547.215 |
| Soggetto topico |
Phase-transfer catalysis
Asymmetry (Chemistry) |
| ISBN |
1-281-94695-8
9786611946951 3-527-62262-4 3-527-62263-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric Phase Transfer Catalysis; Contents; Preface; List of Contributors; 1 The Basic Principle of Phase-Transfer Catalysis and Some Mechanistic Aspects; 1.1 Introduction; 1.2 Inorganic Base-Promoted Activation of Acidic Organic Compounds; 1.2.1 Generation of Reactive Onium Carbanion Species; 1.2.2 Stability of the Onium Carbanion; 1.2.3 Reactivity of the Onium Carbanion; 1.2.4 Nuclueophilic Substitution Reaction; 1.2.5 Nucleophilic Addition to Electrophilic C=X Double Bonds; 1.3 Phase-Transfer-Catalyzed Addition of Anion Supplied as Metal Salt
1.4 Use of Crown Ether as Phase-Transfer CatalystReferences; 2 Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis; 2.1 Introduction; 2.2 α-Amino Acid Synthesis; 2.2.1 Monoalkylation of Schiff Bases Derived from Glycine; 2.2.2 Alkylation of Schiff Bases Derived from α-Alkyl-α-Amino Acids; 2.2.3 Other Alkylations for α-Amino Acid Synthesis; 2.2.4 Michael Reaction of Glycinate Benzophenone Schiff Bases; 2.2.5 Aldol and Related Reactions; 2.2.6 Aza-Henry Reaction; 2.2.7 Strecker Reaction; 2.2.8 Aziridination; 2.2.9 Radical Reaction; 2.3 β-Amino Acid Synthesis 2.3.1 Mannich Reaction2.3.2 Cyclopropanation; 2.4 Conclusions; References; 3 Cinchona-Derived Chiral Phase-Transfer Catalysts for Other Asymmetric Synthesis; 3.1 Introduction; 3.2 Asymmetric Darzens Reaction; 3.3 Asymmetric Conjugated Addition; 3.4 Asymmetric Aldol Reaction; 3.5 Asymmetric Oxygen-Functionalization; 3.6 Asymmetric Alkylation; 3.7 Asymmetric Alkenylation and Alkynylation; 3.8 Asymmetric S(N) Aromatic Reaction; 3.9 Asymmetric Strecker Synthesis; 3.10 Asymmetric Fluorination; References; 4 Cinchona-Derived Chiral Poly(Phase-Transfer Catalysts) for Asymmetric Synthesis 4.1 Cinchona Alkaloids4.1.1 Cinchona Alkaloids in Asymmetric Phase-Transfer Catalysis; 4.1.2 The Origin of Stereoselectivity of Cinchona-PTCs; 4.2 Development of Dimeric Cinchona-PTCs by the Park-Jew Group; 4.2.1 Dimeric Cinchona-PTCs with Phenyl Linker; 4.2.2 1,3-Dimeric Cinchona-PTCs with Electronically Modified Phenyl Linker; 4.2.3 Polymeric Cinchona-PTCs with Other Linkers; 4.2.4 1,3-Phenyl- and 2,7-Naphthyl-Linked Dimeric Cinchona-PTCs; 4.3 Polymeric PTCs Developed by the Najera Group; 4.4 Polymeric PTCs Developed by the Siva Group; 4.5 Polymeric PTCs Developed by the Wang Group 4.6 Asymmetric Epoxidation with Polymeric Cinchona-PTCs4.7 Conclusions; References; 5 Binaphthyl- and Biphenyl-Modified Chiral Phase-Transfer Catalysts for Asymmetric Synthesis; 5.1 Introduction; 5.2 Alkylation; 5.2.1 Asymmetric Synthesis of α-Alkyl α-Amino Acids and Their Derivatives; 5.2.1.1 Asymmetric Monoalkylation of Glycine Ester Schiff Bases; 5.2.1.2 Asymmetric Monoalkylation of Glycine Amide Schiff Bases; 5.2.1.3 Diastereoselective Alkylation of Glycine Schiff Base with Optically Enriched Alkyl Halides; 5.2.1.4 Recyclable Catalysts and Reagents and Solid-Phase Synthesis 5.2.1.5 Application of Asymmetric Synthesis of α-Amino Acids |
| Record Nr. | UNINA-9910144450503321 |
| Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric phase transfer catalysis / / edited by Keiji Maruoka
| Asymmetric phase transfer catalysis / / edited by Keiji Maruoka |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 |
| Descrizione fisica | 1 online resource (230 p.) |
| Disciplina | 547.215 |
| Soggetto topico |
Phase-transfer catalysis
Asymmetry (Chemistry) |
| ISBN |
1-281-94695-8
9786611946951 3-527-62262-4 3-527-62263-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric Phase Transfer Catalysis; Contents; Preface; List of Contributors; 1 The Basic Principle of Phase-Transfer Catalysis and Some Mechanistic Aspects; 1.1 Introduction; 1.2 Inorganic Base-Promoted Activation of Acidic Organic Compounds; 1.2.1 Generation of Reactive Onium Carbanion Species; 1.2.2 Stability of the Onium Carbanion; 1.2.3 Reactivity of the Onium Carbanion; 1.2.4 Nuclueophilic Substitution Reaction; 1.2.5 Nucleophilic Addition to Electrophilic C=X Double Bonds; 1.3 Phase-Transfer-Catalyzed Addition of Anion Supplied as Metal Salt
1.4 Use of Crown Ether as Phase-Transfer CatalystReferences; 2 Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis; 2.1 Introduction; 2.2 α-Amino Acid Synthesis; 2.2.1 Monoalkylation of Schiff Bases Derived from Glycine; 2.2.2 Alkylation of Schiff Bases Derived from α-Alkyl-α-Amino Acids; 2.2.3 Other Alkylations for α-Amino Acid Synthesis; 2.2.4 Michael Reaction of Glycinate Benzophenone Schiff Bases; 2.2.5 Aldol and Related Reactions; 2.2.6 Aza-Henry Reaction; 2.2.7 Strecker Reaction; 2.2.8 Aziridination; 2.2.9 Radical Reaction; 2.3 β-Amino Acid Synthesis 2.3.1 Mannich Reaction2.3.2 Cyclopropanation; 2.4 Conclusions; References; 3 Cinchona-Derived Chiral Phase-Transfer Catalysts for Other Asymmetric Synthesis; 3.1 Introduction; 3.2 Asymmetric Darzens Reaction; 3.3 Asymmetric Conjugated Addition; 3.4 Asymmetric Aldol Reaction; 3.5 Asymmetric Oxygen-Functionalization; 3.6 Asymmetric Alkylation; 3.7 Asymmetric Alkenylation and Alkynylation; 3.8 Asymmetric S(N) Aromatic Reaction; 3.9 Asymmetric Strecker Synthesis; 3.10 Asymmetric Fluorination; References; 4 Cinchona-Derived Chiral Poly(Phase-Transfer Catalysts) for Asymmetric Synthesis 4.1 Cinchona Alkaloids4.1.1 Cinchona Alkaloids in Asymmetric Phase-Transfer Catalysis; 4.1.2 The Origin of Stereoselectivity of Cinchona-PTCs; 4.2 Development of Dimeric Cinchona-PTCs by the Park-Jew Group; 4.2.1 Dimeric Cinchona-PTCs with Phenyl Linker; 4.2.2 1,3-Dimeric Cinchona-PTCs with Electronically Modified Phenyl Linker; 4.2.3 Polymeric Cinchona-PTCs with Other Linkers; 4.2.4 1,3-Phenyl- and 2,7-Naphthyl-Linked Dimeric Cinchona-PTCs; 4.3 Polymeric PTCs Developed by the Najera Group; 4.4 Polymeric PTCs Developed by the Siva Group; 4.5 Polymeric PTCs Developed by the Wang Group 4.6 Asymmetric Epoxidation with Polymeric Cinchona-PTCs4.7 Conclusions; References; 5 Binaphthyl- and Biphenyl-Modified Chiral Phase-Transfer Catalysts for Asymmetric Synthesis; 5.1 Introduction; 5.2 Alkylation; 5.2.1 Asymmetric Synthesis of α-Alkyl α-Amino Acids and Their Derivatives; 5.2.1.1 Asymmetric Monoalkylation of Glycine Ester Schiff Bases; 5.2.1.2 Asymmetric Monoalkylation of Glycine Amide Schiff Bases; 5.2.1.3 Diastereoselective Alkylation of Glycine Schiff Base with Optically Enriched Alkyl Halides; 5.2.1.4 Recyclable Catalysts and Reagents and Solid-Phase Synthesis 5.2.1.5 Application of Asymmetric Synthesis of α-Amino Acids |
| Record Nr. | UNINA-9910829867903321 |
| Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric Synthesis of Natural Products
| Asymmetric Synthesis of Natural Products |
| Autore | Koskinen Ari M. P |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | New York : , : John Wiley & Sons, Incorporated, , 2012 |
| Descrizione fisica | 1 online resource (324 pages) |
| Disciplina | 547.2 |
| Soggetto topico |
Natural products -- Synthesis
Asymmetry (Chemistry) |
| Soggetto genere / forma | Electronic books. |
| ISBN |
9781118347324
9781118347300 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Asymmetric Synthesis of Natural Products -- Contents -- Preface to the First Edition -- Preface to the Second Edition -- List of Common Abbreviations -- Chapter 1 Introduction -- 1.1 Some properties of natural products -- 1.2 Natural products as drugs -- 1.3 Structures of natural products -- 1.4 Asymmetric synthesis of natural products -- 1.5 Synthetic organic chemistry -- References -- Chapter 2 Chirality, Topology, and Asymmetric Synthesis -- 2.1 The need for enantiopure compounds -- 2.2 Determination of enantiomeric purity -- 2.3 Chirality and thermodynamic principles of asymmetric induction -- 2.4 Methods for obtaining chiral compounds -- References -- Chapter 3 Asymmetric Synthesis -- 3.1 Allylic strain -- 3.2 Reactions of the carbonyl group -- 3.2.1 Nucleophilic additions on the carbonyl carbon -- 3.2.2 Reactions at the α-carbon (enolate chemistry) -- 3.2.3 Reactions at the β-carbon of an enone -- 3.3 Reactions of olefins -- 3.3.1 Oxidation -- References -- Chapter 4 Sugars -- 4.1 Monosaccharides -- 4.1.1 Aldoses and ketoses -- 4.1.2 Deoxy sugars -- 4.1.3 Amino sugars -- 4.1.4 Sugar alcohols -- 4.1.5 Acidic sugars -- 4.2 Polysaccharides -- 4.3 Glycoproteins and proteoglycans -- 4.4 Glycolipids -- 4.5 Sugar antibiotics -- 4.6 Cyclitols -- References -- Chapter 5 Amino Acids, Peptides, and Proteins -- 5.1 Amino acids -- 5.2 Peptides and proteins -- 5.3 Enzymes and receptors -- 5.4 Chemical modifications of peptides -- 5.5 Biosynthesis of amino acids -- 5.6 Asymmetric synthesis of amino acids -- 5.6.1 α-Alkylation -- 5.6.2 Amination of ester enolates -- 5.6.3 Catalytic hydrogenation -- 5.6.4 Miscellaneous -- 5.6.5 Pepstatins -- References -- Chapter 6 Nucleosides, Nucleotides, and Nucleic Acids -- References -- Chapter 7 Polyketides -- 7.1 Biosynthesis -- 7.2 Fatty acids -- 7.2.1 Prostaglandins, thromboxanes, and leukotrienes.
7.2.2 Sphingolipids -- 7.3 Polypropionates -- 7.3.1 Polyether antibiotics -- 7.3.2 Macrolides -- 7.3.3 Spiroketals -- 7.4 Aromatic polyketides -- References -- Chapter 8 Terpenes -- 8.1 Terpenes -- 8.1.1 Monoterpenes -- 8.1.2 Sesquiterpenes -- 8.1.3 Diterpenes -- 8.1.4 Higher terpenes -- 8.2 Carotenoids -- 8.3 Steroids -- 8.3.1 Biosynthesis of steroids -- 8.3.2 Asymmetric synthesis of steroids -- References -- Chapter 9 Shikimic Acid Derivatives -- 9.1 Case synthesis: Oseltamivir -- References -- Chapter 10 Alkaloids -- 10.1 Heterocyclic alkaloids -- 10.1.1 Indole alkaloids -- 10.1.2 Pyrrolidine and tropane alkaloids -- 10.1.3 Quinoline and isoquinoline alkaloids -- 10.1.4 Izidine alkaloids -- 10.2 Alkaloids with exocyclic nitrogen -- 10.3 Polyamine alkaloids -- 10.4 Peptide alkaloids -- 10.5 Terpene alkaloids -- References -- Index. |
| Record Nr. | UNINA-9910795983203321 |
|
Koskinen Ari M. P
|
||
| New York : , : John Wiley & Sons, Incorporated, , 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric Synthesis of Natural Products
| Asymmetric Synthesis of Natural Products |
| Autore | Koskinen Ari M. P |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | New York : , : John Wiley & Sons, Incorporated, , 2012 |
| Descrizione fisica | 1 online resource (324 pages) |
| Disciplina | 547.2 |
| Soggetto topico |
Natural products -- Synthesis
Asymmetry (Chemistry) |
| Soggetto genere / forma | Electronic books. |
| ISBN |
9781118347324
9781118347300 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Asymmetric Synthesis of Natural Products -- Contents -- Preface to the First Edition -- Preface to the Second Edition -- List of Common Abbreviations -- Chapter 1 Introduction -- 1.1 Some properties of natural products -- 1.2 Natural products as drugs -- 1.3 Structures of natural products -- 1.4 Asymmetric synthesis of natural products -- 1.5 Synthetic organic chemistry -- References -- Chapter 2 Chirality, Topology, and Asymmetric Synthesis -- 2.1 The need for enantiopure compounds -- 2.2 Determination of enantiomeric purity -- 2.3 Chirality and thermodynamic principles of asymmetric induction -- 2.4 Methods for obtaining chiral compounds -- References -- Chapter 3 Asymmetric Synthesis -- 3.1 Allylic strain -- 3.2 Reactions of the carbonyl group -- 3.2.1 Nucleophilic additions on the carbonyl carbon -- 3.2.2 Reactions at the α-carbon (enolate chemistry) -- 3.2.3 Reactions at the β-carbon of an enone -- 3.3 Reactions of olefins -- 3.3.1 Oxidation -- References -- Chapter 4 Sugars -- 4.1 Monosaccharides -- 4.1.1 Aldoses and ketoses -- 4.1.2 Deoxy sugars -- 4.1.3 Amino sugars -- 4.1.4 Sugar alcohols -- 4.1.5 Acidic sugars -- 4.2 Polysaccharides -- 4.3 Glycoproteins and proteoglycans -- 4.4 Glycolipids -- 4.5 Sugar antibiotics -- 4.6 Cyclitols -- References -- Chapter 5 Amino Acids, Peptides, and Proteins -- 5.1 Amino acids -- 5.2 Peptides and proteins -- 5.3 Enzymes and receptors -- 5.4 Chemical modifications of peptides -- 5.5 Biosynthesis of amino acids -- 5.6 Asymmetric synthesis of amino acids -- 5.6.1 α-Alkylation -- 5.6.2 Amination of ester enolates -- 5.6.3 Catalytic hydrogenation -- 5.6.4 Miscellaneous -- 5.6.5 Pepstatins -- References -- Chapter 6 Nucleosides, Nucleotides, and Nucleic Acids -- References -- Chapter 7 Polyketides -- 7.1 Biosynthesis -- 7.2 Fatty acids -- 7.2.1 Prostaglandins, thromboxanes, and leukotrienes.
7.2.2 Sphingolipids -- 7.3 Polypropionates -- 7.3.1 Polyether antibiotics -- 7.3.2 Macrolides -- 7.3.3 Spiroketals -- 7.4 Aromatic polyketides -- References -- Chapter 8 Terpenes -- 8.1 Terpenes -- 8.1.1 Monoterpenes -- 8.1.2 Sesquiterpenes -- 8.1.3 Diterpenes -- 8.1.4 Higher terpenes -- 8.2 Carotenoids -- 8.3 Steroids -- 8.3.1 Biosynthesis of steroids -- 8.3.2 Asymmetric synthesis of steroids -- References -- Chapter 9 Shikimic Acid Derivatives -- 9.1 Case synthesis: Oseltamivir -- References -- Chapter 10 Alkaloids -- 10.1 Heterocyclic alkaloids -- 10.1.1 Indole alkaloids -- 10.1.2 Pyrrolidine and tropane alkaloids -- 10.1.3 Quinoline and isoquinoline alkaloids -- 10.1.4 Izidine alkaloids -- 10.2 Alkaloids with exocyclic nitrogen -- 10.3 Polyamine alkaloids -- 10.4 Peptide alkaloids -- 10.5 Terpene alkaloids -- References -- Index. |
| Record Nr. | UNINA-9910822697503321 |
|
Koskinen Ari M. P
|
||
| New York : , : John Wiley & Sons, Incorporated, , 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Asymmetric synthesis of natural products / Ari Koskinen
| Asymmetric synthesis of natural products / Ari Koskinen |
| Autore | Koskinen, Ari |
| Pubbl/distr/stampa | Chichester : John Wiley & Sons, c1993 |
| Descrizione fisica | xiii, 234 p. : ill. ; 25 cm |
| Disciplina | 547.7 |
| Soggetto topico |
Asymmetry (Chemistry)
Natural products - Synthesis |
| ISBN | 0471938483 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISALENTO-991003424229707536 |
|
Koskinen, Ari
|
||
| Chichester : John Wiley & Sons, c1993 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
| ||
Chiral ferrocenes in asymmetric catalysis
| Chiral ferrocenes in asymmetric catalysis |
| Autore | Dai Li-xin |
| Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 2010 |
| Disciplina | 547.05621 |
| Soggetto topico |
Ferrocene
Chirality Catalysis Asymmetry (Chemistry) Chemistry Physical Sciences & Mathematics Organic Chemistry |
| ISBN | 3-527-62884-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910140166403321 |
|
Dai Li-xin
|
||
| [Place of publication not identified], : Wiley VCH, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chiral ferrocenes in asymmetric catalysis
| Chiral ferrocenes in asymmetric catalysis |
| Autore | Dai Li-xin |
| Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 2010 |
| Disciplina | 547.05621 |
| Soggetto topico |
Ferrocene
Chirality Catalysis Asymmetry (Chemistry) Chemistry Physical Sciences & Mathematics Organic Chemistry |
| ISBN | 3-527-62884-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910830974903321 |
|
Dai Li-xin
|
||
| [Place of publication not identified], : Wiley VCH, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Asymmetry (Chemistry)
(15)
- Chirality (5)
- Catalysis (3)
- Chemistry (3)
- Exobiology (3)