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Biblioteca

MARC Lista (tabellare)
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Autore Wolcan Ezequiel
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (94 p.)
Disciplina 541/.2254
Altri autori (Persone) FélizMario R
Collana Polymer science and technology
Novinka
Soggetto topico Inorganic polymers
Carbonyl compounds
Soggetto genere / forma Electronic books.
ISBN 1-61728-058-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910461749403321
Wolcan Ezequiel  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Autore Wolcan Ezequiel
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (94 p.)
Disciplina 541/.2254
Altri autori (Persone) FélizMario R
Collana Polymer science and technology
Novinka
Soggetto topico Inorganic polymers
Carbonyl compounds
ISBN 1-61728-058-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910790457603321
Wolcan Ezequiel  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Inorganic polymers containing -Re(CO)3L+ pendants [[electronic resource] /] / Ezequiel Wolcan and Mario R. Féliz
Autore Wolcan Ezequiel
Edizione [1st ed.]
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (94 p.)
Disciplina 541/.2254
Altri autori (Persone) FélizMario R
Collana Polymer science and technology
Novinka
Soggetto topico Inorganic polymers
Carbonyl compounds
ISBN 1-61728-058-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intro -- INORGANIC POLYMERS CONTAINING -RE(CO)3L+ PENDANTS -- INORGANIC POLYMERS CONTAINING -RE(CO)3L+ PENDANTS -- LIBRARY OF CONGRESS CATALOGING-IN-PUBLICATION DATA -- CONTENTS -- PREFACE -- Chapter 1: INTRODUCTION -- Chapter 2: SYNTHESIS OF THE POLYMERS -- Chapter 3: SOLVENT EFFECTS ON MORPHOLOGIES: NANOAGGREGATION -- Chapter 4 -- PHOTOPHYSICAL PROPERTIES OF POLYMER (I) -- Chapter 5: LASER POWER, THERMAL AND SOLVENT EFFECTS ON THE PHOTOPHYSICAL PROPERTIES OF POLYMER (II) -- PHOTOCHEMICAL PROPERTIES OF POLYMER (I) -- Chapter 6: BINDING OF CU(II) ESPECIES TO POLYMER (II) -- Chapter 7: LUMINESCENCE QUENCHING BY CU(II) -- Chapter 8: THEORETICAL OUTLINE OF FLUORESCENCE RESONANCE ENERGY TRANSFER (FRET) IN POLYMERS -- Chapter 9: RESONANCE ENERGY TRANSFER IN THE SOLUTION PHASE PHOTOPHYSICS OF POLYMERS (VII)-(IX) -- Chapter 10 -- CONTRASTING INTRASTRAND PHOTOINDUCED PROCESSES IN MACROMOLECULES CONTAINING PENDANT -RE(CO)3(1,10-PHENANTHROLINE)+: ELECTRON VERSUS ENERGY TRANSFER IN POLYMERS (I) AND (X) -- SOLUTION CHEMISTRY -- TIME-RESOLVED SPECTROSCOPY -- QUENCHING REACTIONS -- PHOTOPHYSICS OF THE ELECTRONICALLY EXCITED (X) -- Chapter 11: CONCLUSION -- ACKNOWLEDGMENTS -- REFERENCES -- INDEX -- Blank Page.
Record Nr. UNINA-9910809883203321
Wolcan Ezequiel  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (635 p.)
Disciplina 547
547.036
547.43
Altri autori (Persone) OteraJunzo
Soggetto topico Carbonyl compounds
Soggetto genere / forma Electronic books.
ISBN 1-283-37034-4
9786613370341
3-527-61326-9
3-527-61327-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbonyl-Lewis acid complexes / Takashi Ooi and Keiji Maruoka -- Carbonyl recognition / Susumu Saito and Hisashi Yamamoto -- Pinacol coupling / Gregory C. Fu -- Modern free radical methods for the synthesis of carbonyl compounds / Ilhyong Ryu and Mitsuo Komatsu -- Acyllithium / Shinji Murai and Keiji Iwamoto -- [pi]-facial selectivity in reaction of carbonyls : a computational approach / James M. Coxon and Richard T. Luibrand -- Engineered asymmetric catalysis / Koichi Mikami -- Aldol reaction : methodology and stereochemistry / Erick M. Carreira -- Stereoselective aldol reactions in the synthesis of polyketide natural products / Ian Paterson, Cameron J. Cowden and Debra J. Wallace -- Allylation of carbonyls : methodology and stereochemistry / Scott E. Denmark and Neil G. Almstead -- Recent applications of the allylation reaction to the synthesis of natural products / Sherry R. Chemler and William R. Roush -- Asymmetric Michael-type addition reaction / Kiyoshi Tomioka -- Stereoselective radical reactions / Mukund P. Sibi and Tara R. Ternes -- Activation of carbonyl and related compounds in aqueous media / Shū Kobayashi, Kei Manabe, and Satoshi Nagayama -- Thermo- and photochemical reactions of carbonyl compounds in the solid state / Fumio Toda.
Record Nr. UNINA-9910144283203321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (635 p.)
Disciplina 547
547.036
547.43
Altri autori (Persone) OteraJunzo
Soggetto topico Carbonyl compounds
ISBN 1-283-37034-4
9786613370341
3-527-61326-9
3-527-61327-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbonyl-Lewis acid complexes / Takashi Ooi and Keiji Maruoka -- Carbonyl recognition / Susumu Saito and Hisashi Yamamoto -- Pinacol coupling / Gregory C. Fu -- Modern free radical methods for the synthesis of carbonyl compounds / Ilhyong Ryu and Mitsuo Komatsu -- Acyllithium / Shinji Murai and Keiji Iwamoto -- [pi]-facial selectivity in reaction of carbonyls : a computational approach / James M. Coxon and Richard T. Luibrand -- Engineered asymmetric catalysis / Koichi Mikami -- Aldol reaction : methodology and stereochemistry / Erick M. Carreira -- Stereoselective aldol reactions in the synthesis of polyketide natural products / Ian Paterson, Cameron J. Cowden and Debra J. Wallace -- Allylation of carbonyls : methodology and stereochemistry / Scott E. Denmark and Neil G. Almstead -- Recent applications of the allylation reaction to the synthesis of natural products / Sherry R. Chemler and William R. Roush -- Asymmetric Michael-type addition reaction / Kiyoshi Tomioka -- Stereoselective radical reactions / Mukund P. Sibi and Tara R. Ternes -- Activation of carbonyl and related compounds in aqueous media / Shū Kobayashi, Kei Manabe, and Satoshi Nagayama -- Thermo- and photochemical reactions of carbonyl compounds in the solid state / Fumio Toda.
Record Nr. UNINA-9910829986803321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Modern carbonyl chemistry [[electronic resource] /] / edited by Junzo Otera
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (635 p.)
Disciplina 547
547.036
547.43
Altri autori (Persone) OteraJunzo
Soggetto topico Carbonyl compounds
ISBN 1-283-37034-4
9786613370341
3-527-61326-9
3-527-61327-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbonyl-Lewis acid complexes / Takashi Ooi and Keiji Maruoka -- Carbonyl recognition / Susumu Saito and Hisashi Yamamoto -- Pinacol coupling / Gregory C. Fu -- Modern free radical methods for the synthesis of carbonyl compounds / Ilhyong Ryu and Mitsuo Komatsu -- Acyllithium / Shinji Murai and Keiji Iwamoto -- [pi]-facial selectivity in reaction of carbonyls : a computational approach / James M. Coxon and Richard T. Luibrand -- Engineered asymmetric catalysis / Koichi Mikami -- Aldol reaction : methodology and stereochemistry / Erick M. Carreira -- Stereoselective aldol reactions in the synthesis of polyketide natural products / Ian Paterson, Cameron J. Cowden and Debra J. Wallace -- Allylation of carbonyls : methodology and stereochemistry / Scott E. Denmark and Neil G. Almstead -- Recent applications of the allylation reaction to the synthesis of natural products / Sherry R. Chemler and William R. Roush -- Asymmetric Michael-type addition reaction / Kiyoshi Tomioka -- Stereoselective radical reactions / Mukund P. Sibi and Tara R. Ternes -- Activation of carbonyl and related compounds in aqueous media / Shū Kobayashi, Kei Manabe, and Satoshi Nagayama -- Thermo- and photochemical reactions of carbonyl compounds in the solid state / Fumio Toda.
Record Nr. UNINA-9910840676403321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (367 p.)
Disciplina 547.036
547.05621046
Altri autori (Persone) TakedaTakeshi
Soggetto topico Carbonyl compounds
ISBN 1-280-52047-7
9786610520473
3-527-60538-X
3-527-60188-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Carbonyl Olefination; Contents; Preface; List of Authors; 1 The Wittig Reaction; 1.1 Introduction; 1.2 The ""Classic"" Wittig Reaction; 1.2.1 Mechanism and Stereoselectivity; 1.2.2 Nature of the Ylide and Carbonyl Compound; 1.2.3 Reagents and Reaction Conditions; 1.3 Horner-Wadsworth-Emmons Reaction; 1.3.1 Mechanism and Stereochemistry; 1.3.2 Reagents and Reaction Conditions; 1.4 Horner-Wittig (HW) Reaction; 1.4.1 Mechanism and Stereochemistry; 1.4.2 Reagents and Reaction Conditions; 1.5 Conclusion; References; 2 The Peterson and Related Reactions; 2.1 Introduction
2.2 Stereochemistry and the Reaction Mechanism of the Peterson Reaction2.2.1 Stereochemistry and the Reaction Mechanism of the Peterson Reaction of β-Hydroxyalkylsilanes; 2.2.1.1 Stepwise Mechanism; 2.2.1.2 Reaction Mechanism via a 1,2-Oxasiletanide; 2.2.2 Reaction Mechanism of the Addition Step of an α-Silyl Carbanion to a Carbonyl Compound; 2.2.2.1 Approach Control of the Transition State; 2.2.2.2 Concerted Mechanism; 2.2.2.3 Chelation Control Mechanism; 2.2.3 Theoretical Calculations on the Reaction Mechanism; 2.2.4 Convergently Stereoselective Peterson Reactions
2.3 Generation of α-Silyl Carbanions and their Peterson Reactions2.3.1 Generation of α-Silyl Carbanions from α-Silylalkyl Halides; 2.3.1.1 Generation of α-Silyl Grignard Reagents from α-Silylalkyl Halides; 2.3.1.2 Generation of α-Silyl Alkyllithium Reagents from α-Silylalkyl Halides; 2.3.1.3 Synthesis of Terminal Alkenes by the Use of α-Silyl Carbanions Generated from α-Silylalkyl Halides; 2.3.1.4 Reactions of α-Silyl Carbanions Generated from α-Silylalkyl Halides with Esters, Carboxylic Acids, and Acetals; 2.3.1.5 The Reformatsky-Peterson Reactions of α-Silylalkyl Halides
2.3.2 Generation of α-Silyl Carbanions by Deprotonation of Alkylsilanes2.3.2.1 Generation of α-Silyl Carbanions Bearing an Aryl or a Heteroaryl Group; 2.3.2.2 Generation of α-Silyl Carbanions Bearing an Alkoxy Group; 2.3.2.3 Generation of α-Silyl Carbanions Bearing a Nitrogen-Containing Group; 2.3.2.4 Generation of α-Silyl Carbanions Bearing a Sulfur-Containing Group; 2.3.2.5 Generation of α-Silyl Carbanions Bearing a Phosphorus-Containing Group; 2.3.2.6 Generation of α-Silyl Carbanions Bearing a Halogen Group; 2.3.2.7 Generation of α-Silyl Carbanions from α-Silyl Ketones
2.3.2.8 Generation of α-Silyl Carbanions Bearing an Ester Group2.3.2.9 Generation of α-Silyl Carbanions Bearing a Lactone Group; 2.3.2.10 Generation of α-Silyl Carbanions Bearing Thiocarboxylate or Dithiocarboxylate Ester Groups; 2.3.2.11 Generation of α-Silyl Carbanions Bearing an Imino Group; 2.3.2.12 Generation of α-Silyl Carbanions Bearing an Amide Group; 2.3.2.13 Generation of α-Silyl Carbanions Bearing a Cyano Group; 2.3.2.14 Generation of α-Silyl Carbanions from Allylsilanes; 2.3.2.15 Generation of α-Silyl Carbanions from Propargylsilanes
2.3.3 Generation of α-Silyl Carbanions by Substitution of a Heteroatom
Record Nr. UNINA-9910146238103321
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (367 p.)
Disciplina 547.036
547.05621046
Altri autori (Persone) TakedaTakeshi
Soggetto topico Carbonyl compounds
ISBN 1-280-52047-7
9786610520473
3-527-60538-X
3-527-60188-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Carbonyl Olefination; Contents; Preface; List of Authors; 1 The Wittig Reaction; 1.1 Introduction; 1.2 The ""Classic"" Wittig Reaction; 1.2.1 Mechanism and Stereoselectivity; 1.2.2 Nature of the Ylide and Carbonyl Compound; 1.2.3 Reagents and Reaction Conditions; 1.3 Horner-Wadsworth-Emmons Reaction; 1.3.1 Mechanism and Stereochemistry; 1.3.2 Reagents and Reaction Conditions; 1.4 Horner-Wittig (HW) Reaction; 1.4.1 Mechanism and Stereochemistry; 1.4.2 Reagents and Reaction Conditions; 1.5 Conclusion; References; 2 The Peterson and Related Reactions; 2.1 Introduction
2.2 Stereochemistry and the Reaction Mechanism of the Peterson Reaction2.2.1 Stereochemistry and the Reaction Mechanism of the Peterson Reaction of β-Hydroxyalkylsilanes; 2.2.1.1 Stepwise Mechanism; 2.2.1.2 Reaction Mechanism via a 1,2-Oxasiletanide; 2.2.2 Reaction Mechanism of the Addition Step of an α-Silyl Carbanion to a Carbonyl Compound; 2.2.2.1 Approach Control of the Transition State; 2.2.2.2 Concerted Mechanism; 2.2.2.3 Chelation Control Mechanism; 2.2.3 Theoretical Calculations on the Reaction Mechanism; 2.2.4 Convergently Stereoselective Peterson Reactions
2.3 Generation of α-Silyl Carbanions and their Peterson Reactions2.3.1 Generation of α-Silyl Carbanions from α-Silylalkyl Halides; 2.3.1.1 Generation of α-Silyl Grignard Reagents from α-Silylalkyl Halides; 2.3.1.2 Generation of α-Silyl Alkyllithium Reagents from α-Silylalkyl Halides; 2.3.1.3 Synthesis of Terminal Alkenes by the Use of α-Silyl Carbanions Generated from α-Silylalkyl Halides; 2.3.1.4 Reactions of α-Silyl Carbanions Generated from α-Silylalkyl Halides with Esters, Carboxylic Acids, and Acetals; 2.3.1.5 The Reformatsky-Peterson Reactions of α-Silylalkyl Halides
2.3.2 Generation of α-Silyl Carbanions by Deprotonation of Alkylsilanes2.3.2.1 Generation of α-Silyl Carbanions Bearing an Aryl or a Heteroaryl Group; 2.3.2.2 Generation of α-Silyl Carbanions Bearing an Alkoxy Group; 2.3.2.3 Generation of α-Silyl Carbanions Bearing a Nitrogen-Containing Group; 2.3.2.4 Generation of α-Silyl Carbanions Bearing a Sulfur-Containing Group; 2.3.2.5 Generation of α-Silyl Carbanions Bearing a Phosphorus-Containing Group; 2.3.2.6 Generation of α-Silyl Carbanions Bearing a Halogen Group; 2.3.2.7 Generation of α-Silyl Carbanions from α-Silyl Ketones
2.3.2.8 Generation of α-Silyl Carbanions Bearing an Ester Group2.3.2.9 Generation of α-Silyl Carbanions Bearing a Lactone Group; 2.3.2.10 Generation of α-Silyl Carbanions Bearing Thiocarboxylate or Dithiocarboxylate Ester Groups; 2.3.2.11 Generation of α-Silyl Carbanions Bearing an Imino Group; 2.3.2.12 Generation of α-Silyl Carbanions Bearing an Amide Group; 2.3.2.13 Generation of α-Silyl Carbanions Bearing a Cyano Group; 2.3.2.14 Generation of α-Silyl Carbanions from Allylsilanes; 2.3.2.15 Generation of α-Silyl Carbanions from Propargylsilanes
2.3.3 Generation of α-Silyl Carbanions by Substitution of a Heteroatom
Record Nr. UNINA-9910830654803321
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Modern carbonyl olefination [[electronic resource] /] / Takeshi Takeda (ed.)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (367 p.)
Disciplina 547.036
547.05621046
Altri autori (Persone) TakedaTakeshi
Soggetto topico Carbonyl compounds
ISBN 1-280-52047-7
9786610520473
3-527-60538-X
3-527-60188-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Carbonyl Olefination; Contents; Preface; List of Authors; 1 The Wittig Reaction; 1.1 Introduction; 1.2 The ""Classic"" Wittig Reaction; 1.2.1 Mechanism and Stereoselectivity; 1.2.2 Nature of the Ylide and Carbonyl Compound; 1.2.3 Reagents and Reaction Conditions; 1.3 Horner-Wadsworth-Emmons Reaction; 1.3.1 Mechanism and Stereochemistry; 1.3.2 Reagents and Reaction Conditions; 1.4 Horner-Wittig (HW) Reaction; 1.4.1 Mechanism and Stereochemistry; 1.4.2 Reagents and Reaction Conditions; 1.5 Conclusion; References; 2 The Peterson and Related Reactions; 2.1 Introduction
2.2 Stereochemistry and the Reaction Mechanism of the Peterson Reaction2.2.1 Stereochemistry and the Reaction Mechanism of the Peterson Reaction of β-Hydroxyalkylsilanes; 2.2.1.1 Stepwise Mechanism; 2.2.1.2 Reaction Mechanism via a 1,2-Oxasiletanide; 2.2.2 Reaction Mechanism of the Addition Step of an α-Silyl Carbanion to a Carbonyl Compound; 2.2.2.1 Approach Control of the Transition State; 2.2.2.2 Concerted Mechanism; 2.2.2.3 Chelation Control Mechanism; 2.2.3 Theoretical Calculations on the Reaction Mechanism; 2.2.4 Convergently Stereoselective Peterson Reactions
2.3 Generation of α-Silyl Carbanions and their Peterson Reactions2.3.1 Generation of α-Silyl Carbanions from α-Silylalkyl Halides; 2.3.1.1 Generation of α-Silyl Grignard Reagents from α-Silylalkyl Halides; 2.3.1.2 Generation of α-Silyl Alkyllithium Reagents from α-Silylalkyl Halides; 2.3.1.3 Synthesis of Terminal Alkenes by the Use of α-Silyl Carbanions Generated from α-Silylalkyl Halides; 2.3.1.4 Reactions of α-Silyl Carbanions Generated from α-Silylalkyl Halides with Esters, Carboxylic Acids, and Acetals; 2.3.1.5 The Reformatsky-Peterson Reactions of α-Silylalkyl Halides
2.3.2 Generation of α-Silyl Carbanions by Deprotonation of Alkylsilanes2.3.2.1 Generation of α-Silyl Carbanions Bearing an Aryl or a Heteroaryl Group; 2.3.2.2 Generation of α-Silyl Carbanions Bearing an Alkoxy Group; 2.3.2.3 Generation of α-Silyl Carbanions Bearing a Nitrogen-Containing Group; 2.3.2.4 Generation of α-Silyl Carbanions Bearing a Sulfur-Containing Group; 2.3.2.5 Generation of α-Silyl Carbanions Bearing a Phosphorus-Containing Group; 2.3.2.6 Generation of α-Silyl Carbanions Bearing a Halogen Group; 2.3.2.7 Generation of α-Silyl Carbanions from α-Silyl Ketones
2.3.2.8 Generation of α-Silyl Carbanions Bearing an Ester Group2.3.2.9 Generation of α-Silyl Carbanions Bearing a Lactone Group; 2.3.2.10 Generation of α-Silyl Carbanions Bearing Thiocarboxylate or Dithiocarboxylate Ester Groups; 2.3.2.11 Generation of α-Silyl Carbanions Bearing an Imino Group; 2.3.2.12 Generation of α-Silyl Carbanions Bearing an Amide Group; 2.3.2.13 Generation of α-Silyl Carbanions Bearing a Cyano Group; 2.3.2.14 Generation of α-Silyl Carbanions from Allylsilanes; 2.3.2.15 Generation of α-Silyl Carbanions from Propargylsilanes
2.3.3 Generation of α-Silyl Carbanions by Substitution of a Heteroatom
Record Nr. UNINA-9910841032103321
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Autore Cotarca L (Livius)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (670 p.)
Disciplina 661.06812
661.891
Altri autori (Persone) EckertH (Heiner)
Soggetto topico Phosgene
Carbonyl compounds
ISBN 1-280-52018-3
9786610520183
3-527-60503-7
3-527-60262-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Phosgenations - A Handbook; Contents; Preface; 1 Contradictions; References; 2 Phosgenation Reagents; 2.1 Phosgene; 2.1.1 Conventional Manufacturing Processes; 2.1.2 Manufacturing Processes "On Demand of Consumer"; 2.2 Phosgene "Oligomers"; 2.2.1 Diphosgene; 2.2.2 Triphosgene; 2.2.2.1 Triphosgene as a Phosgene Equivalent or Phosgene Source; 2.2.2.2 Stability: Thermally and Chemically Induced Decomposition; 2.2.2.3 Preparation; 2.3 Other Phosgene Equivalents and Substitutes; 2.3.1 Oxalyl Chloride; 2.3.2 1,1-Carbonyldiimidazole; 2.3.3 Dimethyl Carbonate (DMC); 2.4 References
3 Evaluation of Phosgenation Reagents3.1 Definition; 3.2 Reactivity; 3.3 Physical Properties; 3.4 Physiological Data; 3.5 References; 4 Phosgenation Reactions; 4.1 Classification of Phosgenation Reactions; 4.2 Chloroformylation (Chlorocarbonylation); 4.2.1 Chloroformates (Chlorocarbonylation of Alcohols); 4.2.2 Carbamoyl Chlorides (Chlorocarbonylation of Amines); 4.2.2.1 Reactions with Primary Amines; 4.2.2.2 Reactions with Secondary Amines; 4.2.2.3 Reactions with Tertiary Amines; 4.2.2.4 Reactions with Amides; 4.3 Carbonylation; 4.3.1 Isocyanates; 4.3.1.1 Introduction
4.3.1.2 Aromatic Isocyanates4.3.1.3 Alkyl and Alkenyl Isocyanates; 4.3.1.4 Heterocyclic Isocyanates; 4.3.1.5 Isocyanates of Amino Acids; 4.3.1.6 Acyl Isocyanates; 4.3.1.7 Silane Isocyanates; 4.3.2 Carbamates; 4.3.2.1 Phosgene and Haloformates as Reagents; 4.3.2.2 Carbamates Prepared with Isocyanates or Carbamoyl Chlorides; 4.3.2.3 Carbamates Prepared with N,N ́-Carbonyldiimidazole (CDI); 4.3.2.4 Carbamates by Aminolysis of Carbonate or Dithiocarbonate Esters; 4.3.2.5 Enol Carbamates; 4.3.2.6 Carbamates from Isocyanides; 4.3.2.7 Potassium Carbonate as a Carbonylating Reagent
4.3.2.8 Carbamates Prepared with Acryloyl Azide4.3.2.9 Carbon Monoxide; 4.3.2.10 Carbon Dioxide; 4.3.2.11 Sodium Nitrite/HCl; 4.3.3 Carbonates; 4.3.3.1 Chloroformates; 4.3.3.2 Phosgene; 4.3.3.3 Diphosgene; 4.3.3.4 Triphosgene; 4.3.3.5 Carbonyldiimidazole (CDI); 4.3.3.6 Acyl Carbonates; 4.3.3.7 Carbonates (Interchanges); 4.3.3.8 Carbon Oxides, CO, CO(2), and MCO(3); 4.3.3.9 Ureas; 4.3.3.10 Enzyme Catalysis; 4.3.4 Ureas; 4.3.4.1 Phosgene and Symmetrical Phosgene Equivalents; 4.3.4.2 Unsymmetrical Phosgene Equivalents; 4.3.4.3 Carbon Monoxide; 4.3.4.4 Carbon Dioxide; 4.3.4.5 Organic Carbonates
4.3.4.6 Aminolysis of S-Methylthiocarbamates Prepared from Carbonimidodithioates4.3.4.7 Diiodosilane Method; 4.3.4.8 N-Alkylation of Simple Ureas; 4.3.4.9 The Reductive Amination of Aldehydes with Monoalkylureas; 4.3.4.10 Catalytic [Ru(PPh(3))(3)] Aminolysis of Formamides; 4.3.4.11 HY Zeolite HSZ-360 Catalyzed Aminolysis of Acetoacetanilides; 4.3.5 Reactions with Binucleophiles; 4.3.5.1 N,O- and N,S-Binucleophiles. Formation of Oxazolidin-2-ones and Thiazolidin-2-ones; 4.3.5.2 N,N-Binucleophiles. Formation of 2-Oxoimidazolidines; 4.3.5.3 O,O-Binucleophiles. Formation of Cyclic Carbonates
4.3.5.4 N,COOH Binucleophiles. Formation of N-Carboxyanhydrides of α-Amino Acids
Record Nr. UNINA-9910146054103321
Cotarca L (Livius)  
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
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