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The chemical biology of nucleic acids [[electronic resource] /] / edited by Günter Mayer
The chemical biology of nucleic acids [[electronic resource] /] / edited by Günter Mayer
Edizione [1st ed.]
Pubbl/distr/stampa Chichester, UK, : Wiley, 2010
Descrizione fisica 1 online resource (496 p.)
Disciplina 547.7
572.8
Altri autori (Persone) MayerGünter <1972->
Soggetto topico Nucleic acids
Biomolecules
ISBN 1-282-68356-X
9786612683565
0-470-66400-2
0-470-66401-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Chemical Biology of Nucleic Acids; Contents; Foreword; Preface; List of Contributors; 1 Chemical Synthesis of Modified RNA; 2 Expansion of the Genetic Alphabet in Nucleic Acids by Creating New Base Pairs; 3 Chemical Biology of DNA Replication: Probing DNA Polymerase Selectivity Mechanisms with Modified Nucleotides; 4 Nucleic Acid-templated Chemistry; 5 Chemical Biology of Peptide Nucleic Acids (PNAs); 6 The Interactions of Small Molecules with DNA and RNA; 7 The Architectural Motifs of Folded RNAs; 8 Genesis and Biological Applications of Locked Nucleic Acids (LNAs)
9 Small Non-coding RNA in Bacteria10 MicroRNA-guided Gene Silencing; 11 Nucleic Acid-based Therapies; 12 Innate Immune Recognition of Nucleic Acids; 13 Light-responsive Nucleic Acids for the Spatiotemporal Control of Biological Processes; 14 DNA Methylation; 15 Frameworks for Programming RNA Devices; 16 RNA as a Catalyst: The Diels-Alderase Ribozyme; 17 Evolving an Understanding of RNA Function by In Vitro Approaches; 18 The Chemical Biology of Aptamers: Synthesis and Applications; 19 Nucleic Acids as Detection Tools; 20 Bacterial Riboswitch Discovery and Analysis; Index; Color Plates
Record Nr. UNINA-9910841568103321
Chichester, UK, : Wiley, 2010
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Chemistry of natural products / Suyata V, Bhat, Bhimsen A. Nagasampagi, Meenakshi Sivakumar
Chemistry of natural products / Suyata V, Bhat, Bhimsen A. Nagasampagi, Meenakshi Sivakumar
Autore Bhat, Suyata V.
Pubbl/distr/stampa Berlin : Springer
Descrizione fisica xxxi, 840 p. : ill. ; 24 cm
Disciplina 547.7
Altri autori (Persone) Bhat, Syiata V.
Sivakumar, Meenakshi
Soggetto topico Natural products
ISBN 3540406697
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991001367829707536
Bhat, Suyata V.  
Berlin : Springer
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The Chemistry of natural products / edited by R. H. Thomson
The Chemistry of natural products / edited by R. H. Thomson
Pubbl/distr/stampa Glasgow : Blackie
Descrizione fisica x, 452 p. : ill. ; 24 cm
Disciplina 547.7
Altri autori (Persone) Thomson, Ronald Hunter
Soggetto topico Natural products
ISBN 0412005514
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991000912639707536
Glasgow : Blackie
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Chemistry of Plant Natural Products [[electronic resource] ] : Stereochemistry, Conformation, Synthesis, Biology, and Medicine / / by Sunil Kumar Talapatra, Bani Talapatra
Chemistry of Plant Natural Products [[electronic resource] ] : Stereochemistry, Conformation, Synthesis, Biology, and Medicine / / by Sunil Kumar Talapatra, Bani Talapatra
Autore Talapatra Sunil Kumar
Edizione [1st ed. 2015.]
Pubbl/distr/stampa Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015
Descrizione fisica 1 online resource (1196 p.)
Disciplina 547.7
Soggetto topico Organic chemistry
Medicinal chemistry
Pharmacology
Biochemistry
Pharmacy
Organic Chemistry
Medicinal Chemistry
Pharmacology/Toxicology
Biochemistry, general
ISBN 3-642-45410-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction: enzymes, cofactors/coenzymes, primary and secondary metabolites, natural products and their functions, plant chemical ecology, biosynthesis, metabolic pathways -- Fundamental Stereochemical Concepts and Nomenclatures -- Important Biological Events Occurring in Plants -- Natural Products Chemistry -- Biosynthesis of Terpenoids, The Oldest Natural Products -- Monoterpenoids (C10) -- Sesquiterpenoids (C15) -- Diterpenoids (C20) -- Sesterpenoids (C25) -- Triterpenes -- Steroids: Cholesterol and Other Phytosterols -- Carotenoids-GGPP Derived Polyisoprenoid (C40) Coloring Pigments -- Shikimic Acid Pathway -- Polyketide Pathway, Biosynthesis of Diverse Clases of Aromatic Compounds -- Alkaloids: General Introduction -- Hygrine, Hygroline and Cuscohygrine (Ornithine-Derived Alkaloids) -- Coniine, Conhydrine and Pseudoconhydrine -- Nicotine -- Atropine [(±)-Hyoscyamine] and Cocaine -- Ephedrine and Pseudoephedrine -- Pilocarpine and Isopilocarpine -- Papaverine -- Morphine, Codeine, Thebaine -- Colchicine -- Quinine: Cinchona Alkalods -- Reserpine -- Strychnine, an Alkaloid with Heptacyclic Dense Molecular Scaffold -- Dimeric Indole Alkaloids:Vinblastine (Vincaleukoblastine), Vineristine (Leurocristine) and Their Derivatives -- Some More Alkaloids Having Diverse Skeletal Patterns -- Important Outcomes of Chemical Studies on Natural Products -- Chiral Recognition in Biological Systems and Natural Chiral Auxiliaries -- Natural Products in the Parlor of Pharmaceuticals -- Organic Phytonutrients and Their Functions -- Appendices.  .
Record Nr. UNINA-9910298628003321
Talapatra Sunil Kumar  
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015
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The chemistry of polymers [[electronic resource] /] / John W. Nicholson
The chemistry of polymers [[electronic resource] /] / John W. Nicholson
Autore Nicholson John W
Edizione [2nd ed.]
Pubbl/distr/stampa Cambridge, : Royal Society of Chemistry, 1997
Descrizione fisica 1 online resource (204 p.)
Disciplina 547.7
Collana RSC paperbacks
Soggetto topico Polymers
Polymerization
Soggetto genere / forma Electronic books.
ISBN 1-84755-207-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto BK9780854045587-FX001; BK9780854045587-FP001; BK9780854045587-FP005; BK9780854045587-FP007; BK9780854045587-00001; BK9780854045587-00027; BK9780854045587-00047; BK9780854045587-00063; BK9780854045587-00077; BK9780854045587-00094; BK9780854045587-00112; BK9780854045587-00139; BK9780854045587-00155; BK9780854045587-00173; BK9780854045587-00183; BK9780854045587-00185
Record Nr. UNINA-9910456708303321
Nicholson John W  
Cambridge, : Royal Society of Chemistry, 1997
Materiale a stampa
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The chemistry of polymers [[electronic resource] /] / John W. Nicholson
The chemistry of polymers [[electronic resource] /] / John W. Nicholson
Autore Nicholson John W
Edizione [2nd ed.]
Pubbl/distr/stampa Cambridge, : Royal Society of Chemistry, 1997
Descrizione fisica 1 online resource (204 p.)
Disciplina 547.7
Collana RSC paperbacks
Soggetto topico Polymers
Polymerization
ISBN 1-84755-207-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto BK9780854045587-FX001; BK9780854045587-FP001; BK9780854045587-FP005; BK9780854045587-FP007; BK9780854045587-00001; BK9780854045587-00027; BK9780854045587-00047; BK9780854045587-00063; BK9780854045587-00077; BK9780854045587-00094; BK9780854045587-00112; BK9780854045587-00139; BK9780854045587-00155; BK9780854045587-00173; BK9780854045587-00183; BK9780854045587-00185
Record Nr. UNINA-9910780938403321
Nicholson John W  
Cambridge, : Royal Society of Chemistry, 1997
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The chemistry of polymers [[electronic resource] /] / John W. Nicholson
The chemistry of polymers [[electronic resource] /] / John W. Nicholson
Autore Nicholson John W
Edizione [2nd ed.]
Pubbl/distr/stampa Cambridge, : Royal Society of Chemistry, 1997
Descrizione fisica 1 online resource (204 p.)
Disciplina 547.7
Collana RSC paperbacks
Soggetto topico Polymers
Polymerization
ISBN 1-84755-207-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto BK9780854045587-FX001; BK9780854045587-FP001; BK9780854045587-FP005; BK9780854045587-FP007; BK9780854045587-00001; BK9780854045587-00027; BK9780854045587-00047; BK9780854045587-00063; BK9780854045587-00077; BK9780854045587-00094; BK9780854045587-00112; BK9780854045587-00139; BK9780854045587-00155; BK9780854045587-00173; BK9780854045587-00183; BK9780854045587-00185
Record Nr. UNINA-9910824987903321
Nicholson John W  
Cambridge, : Royal Society of Chemistry, 1997
Materiale a stampa
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Chromatography, foams, copolymers / with contributions by Y. Doi ... [et al.]
Chromatography, foams, copolymers / with contributions by Y. Doi ... [et al.]
Pubbl/distr/stampa Berlin [etc.] : Springer-Verlag, copyr. 1986
Descrizione fisica 263 p. : 98 ill., 68 tab. ; 24 cm
Disciplina 547.7
Collana Advances in polymer science
Soggetto non controllato copolimeri
ISBN 3-540-15786-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-990000101090203316
Berlin [etc.] : Springer-Verlag, copyr. 1986
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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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
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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
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
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