Bibliography of organic acids in higher plants
| Bibliography of organic acids in higher plants |
| Autore | Buch M. L (Margaret L.) |
| Pubbl/distr/stampa | [Washington D.C.], : Agricultural Research Service, 1957 |
| Descrizione fisica |
1 online resource (100 pages) : illustrations
1 online resource |
| Collana | Agriculture handbook / United States Department of Agriculture |
| Soggetto topico | Organic acids |
| Soggetto genere / forma | Bibliographies. |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910703387603321 |
Buch M. L (Margaret L.)
|
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| [Washington D.C.], : Agricultural Research Service, 1957 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Boronic acids [[electronic resource] ] : preparation and applications in organic synthesis, medicine and materials / / edited by Dennis G. Hall ; with a foreword by Akira Suszuki
| Boronic acids [[electronic resource] ] : preparation and applications in organic synthesis, medicine and materials / / edited by Dennis G. Hall ; with a foreword by Akira Suszuki |
| Edizione | [2nd completely rev. ed.] |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2011 |
| Descrizione fisica | 1 online resource (729 p.) |
| Disciplina | 547.05671 |
| Altri autori (Persone) | HallDennis G. <1968-> |
| Soggetto topico |
Organic acids
Organoboron compounds Organic acids - Therapeutic use Organoboron compounds - Therapeutic use Organic acids - Synthesis Organoboron compounds - Synthesis |
| ISBN |
1-283-60404-3
9786613916495 3-527-33214-6 3-527-63934-9 3-527-63932-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials; Foreword; Contents to Volume 1; Contents to Volume 2; Preface; List of Contributors; 1 Structure, Properties, and Preparation of Boronic Acid Derivatives: Overview of Their Reactions and Applications; 1.1 Introduction and Historical Background; 1.2 Structure and Properties of Boronic Acid Derivatives; 1.2.1 General Types and Nomenclature of Boronic Acid Derivatives; 1.2.2 Boronic Acids; 1.2.2.1 Structure and Bonding; 1.2.2.2 Physical Properties and Handling; 1.2.2.3 Safety Considerations
1.2.2.4 Acidic Character1.2.2.5 Chemical Stability; 1.2.3 Boronic Acid Derivatives; 1.2.3.1 Boroxines (Cyclic Anhydrides); 1.2.3.2 Boronic Esters; 1.2.3.3 Acyloxy- and Diacyloxyboronates; 1.2.3.4 Dialkoxyboranes and Other Heterocyclic Boranes; 1.2.3.5 Diboronyl Esters; 1.2.3.6 Azaborolidines and Other Boron-Nitrogen Heterocycles; 1.2.3.7 Dihaloboranes and Dihydroalkylboranes; 1.2.3.8 Trifluoro- and Trihydroxyborate Salts; 1.3 Preparation of Boronic Acids and Their Esters; 1.3.1 Arylboronic Acids; 1.3.1.1 Electrophilic Trapping of Arylmetal Intermediates with Borates 1.3.1.2 Transmetalation of Aryl Silanes and Stannanes1.3.1.3 Coupling of Aryl Halides with Diboronyl Reagents; 1.3.1.4 Direct Boronation by Transition Metal-Catalyzed Aromatic C-H Functionalization; 1.3.1.5 Cycloadditions of Alkynylboronates; 1.3.1.6 Other Methods; 1.3.2 Diboronic Acids; 1.3.3 Heterocyclic Boronic Acids; 1.3.4 Alkenylboronic Acids; 1.3.4.1 Electrophilic Trapping of Alkenylmetal Intermediates with Borates; 1.3.4.2 Transmetalation Methods; 1.3.4.3 Transition Metal-Catalyzed Coupling between Alkenyl Halides/ Triflates and Diboronyl Reagents; 1.3.4.4 Hydroboration of Alkynes 1.3.4.5 Alkene Metathesis1.3.4.6 Diboronylation and Silaboration of Unsaturated Compounds; 1.3.4.7 Other Methods; 1.3.5 Alkynylboronic Acids; 1.3.6 Alkylboronic Acids; 1.3.7 Allylic Boronic Acids; 1.3.8 Chemoselective Transformations of Compounds Containing a Boronic Acid (Ester) Substituent; 1.3.8.1 Oxidative Methods; 1.3.8.2 Reductive Methods; 1.3.8.3 Generation and Reactions of a-Boronyl-Substituted Carbanions and Radicals; 1.3.8.4 Reactions of a-Haloalkylboronic Esters; 1.3.8.5 Other Transformations; 1.3.8.6 Protection of Boronic Acids for Orthogonal Transformations 1.4 Isolation and Characterization1.4.1 Recrystallization and Chromatography; 1.4.2 Solid Supports for Boronic Acid Immobilization and Purification; 1.4.2.1 Diethanolaminomethyl Polystyrene; 1.4.2.2 Other Solid-Supported Diol Resins; 1.4.3 Analytical and Spectroscopic Methods for Boronic Acid Derivatives; 1.4.3.1 Melting Points, Combustion Analysis, and HPLC; 1.4.3.2 Mass Spectrometry; 1.4.3.3 Nuclear Magnetic Resonance Spectroscopy; 1.4.3.4 Other Spectroscopic Methods; 1.5 Overview of the Reactions of Boronic Acid Derivatives; 1.5.1 Metalation and Metal-Catalyzed Protodeboronation 1.5.2 Oxidative Replacement of Boron |
| Record Nr. | UNINA-9910137968003321 |
| Weinheim, : Wiley-VCH, c2011 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Boronic acids . Volume 2 Preparation and applications in organic synthesis, medicine and materials / / edited by Dennis G. Hall ; with a foreword by Akira Suszuki
| Boronic acids . Volume 2 Preparation and applications in organic synthesis, medicine and materials / / edited by Dennis G. Hall ; with a foreword by Akira Suszuki |
| Edizione | [Second completely revised edition] |
| Pubbl/distr/stampa | Weinheim : , : Wiley-VCH, , [2011] |
| Descrizione fisica | 1 online resource (729 pages) |
| Disciplina | 547.05671 |
| Soggetto topico |
Àcids orgànics
Compostos organobòrics Organic acids Organoboron compounds Organic acids - Therapeutic use Organoboron compounds - Therapeutic use Organic acids - Synthesis Organoboron compounds - Synthesis |
| ISBN |
9786613916495
9781283604048 1283604043 9783527332144 3527332146 9783527639342 3527639349 9783527639328 3527639322 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials; Foreword; Contents to Volume 1; Contents to Volume 2; Preface; List of Contributors; 1 Structure, Properties, and Preparation of Boronic Acid Derivatives: Overview of Their Reactions and Applications; 1.1 Introduction and Historical Background; 1.2 Structure and Properties of Boronic Acid Derivatives; 1.2.1 General Types and Nomenclature of Boronic Acid Derivatives; 1.2.2 Boronic Acids; 1.2.2.1 Structure and Bonding; 1.2.2.2 Physical Properties and Handling; 1.2.2.3 Safety Considerations
1.2.2.4 Acidic Character1.2.2.5 Chemical Stability; 1.2.3 Boronic Acid Derivatives; 1.2.3.1 Boroxines (Cyclic Anhydrides); 1.2.3.2 Boronic Esters; 1.2.3.3 Acyloxy- and Diacyloxyboronates; 1.2.3.4 Dialkoxyboranes and Other Heterocyclic Boranes; 1.2.3.5 Diboronyl Esters; 1.2.3.6 Azaborolidines and Other Boron-Nitrogen Heterocycles; 1.2.3.7 Dihaloboranes and Dihydroalkylboranes; 1.2.3.8 Trifluoro- and Trihydroxyborate Salts; 1.3 Preparation of Boronic Acids and Their Esters; 1.3.1 Arylboronic Acids; 1.3.1.1 Electrophilic Trapping of Arylmetal Intermediates with Borates 1.3.1.2 Transmetalation of Aryl Silanes and Stannanes1.3.1.3 Coupling of Aryl Halides with Diboronyl Reagents; 1.3.1.4 Direct Boronation by Transition Metal-Catalyzed Aromatic C-H Functionalization; 1.3.1.5 Cycloadditions of Alkynylboronates; 1.3.1.6 Other Methods; 1.3.2 Diboronic Acids; 1.3.3 Heterocyclic Boronic Acids; 1.3.4 Alkenylboronic Acids; 1.3.4.1 Electrophilic Trapping of Alkenylmetal Intermediates with Borates; 1.3.4.2 Transmetalation Methods; 1.3.4.3 Transition Metal-Catalyzed Coupling between Alkenyl Halides/ Triflates and Diboronyl Reagents; 1.3.4.4 Hydroboration of Alkynes 1.3.4.5 Alkene Metathesis1.3.4.6 Diboronylation and Silaboration of Unsaturated Compounds; 1.3.4.7 Other Methods; 1.3.5 Alkynylboronic Acids; 1.3.6 Alkylboronic Acids; 1.3.7 Allylic Boronic Acids; 1.3.8 Chemoselective Transformations of Compounds Containing a Boronic Acid (Ester) Substituent; 1.3.8.1 Oxidative Methods; 1.3.8.2 Reductive Methods; 1.3.8.3 Generation and Reactions of a-Boronyl-Substituted Carbanions and Radicals; 1.3.8.4 Reactions of a-Haloalkylboronic Esters; 1.3.8.5 Other Transformations; 1.3.8.6 Protection of Boronic Acids for Orthogonal Transformations 1.4 Isolation and Characterization1.4.1 Recrystallization and Chromatography; 1.4.2 Solid Supports for Boronic Acid Immobilization and Purification; 1.4.2.1 Diethanolaminomethyl Polystyrene; 1.4.2.2 Other Solid-Supported Diol Resins; 1.4.3 Analytical and Spectroscopic Methods for Boronic Acid Derivatives; 1.4.3.1 Melting Points, Combustion Analysis, and HPLC; 1.4.3.2 Mass Spectrometry; 1.4.3.3 Nuclear Magnetic Resonance Spectroscopy; 1.4.3.4 Other Spectroscopic Methods; 1.5 Overview of the Reactions of Boronic Acid Derivatives; 1.5.1 Metalation and Metal-Catalyzed Protodeboronation 1.5.2 Oxidative Replacement of Boron |
| Record Nr. | UNINA-9910817010203321 |
| Weinheim : , : Wiley-VCH, , [2011] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Boronic acids [[electronic resource] ] : preparation and applications in organic synthesis and medicine / / edited by Dennis G. Hall
| Boronic acids [[electronic resource] ] : preparation and applications in organic synthesis and medicine / / edited by Dennis G. Hall |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (577 p.) |
| Disciplina | 547.05671 |
| Altri autori (Persone) | HallDennis |
| Soggetto topico |
Organic acids
Organoboron compounds Organic acids - Therapeutic use Organoboron compounds - Therapeutic use Organic acids - Synthesis Organoboron compounds - Synthesis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-52116-3
9786610521166 3-527-60682-3 3-527-60654-8 1-60119-357-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Boronic Acids; Table of Contents; Preface; List of Authors; List of Abbreviations; 1 Structure, Properties, and Preparation Of Boronic Acid Derivatives. Overview of Their Reactions and Applications; 1.1 Introduction; 1.2 Structure and Properties of Boronic Acid Derivatives; 1.2.1 General Types and Nomenclature of Boronic Acid Derivatives; 1.2.2 Boronic Acids; 1.2.2.1 Structure and Bonding; 1.2.2.2 Physical Properties and Handling; 1.2.2.3 Safety Considerations; 1.2.2.4 Acidic Character; 1.2.2.5 Chemical Stability; 1.2.3 Boronic Acid Derivatives; 1.2.3.1 Boroxines; 1.2.3.2 Boronic Esters
1.2.3.3 Dialkoxyboranes and other Heterocyclic Boranes1.2.3.4 Diboronyl Esters; 1.2.3.5 Azaborolidines and other Boron Heterocycles; 1.2.3.6 Dihaloboranes and Monoalkylboranes; 1.2.3.7 Trifluoroborate Salts; 1.3 Synthesis of Boronic Acids and their Esters; 1.3.1 Arylboronic Acids; 1.3.1.1 Electrophilic Trapping of Arylmetal Intermediates with Borates; 1.3.1.2 Transmetallation of Aryl Silanes and Stannanes; 1.3.1.3 Coupling of Aryl Halides with Diboronyl Reagents; 1.3.1.4 Direct Boronylation by Transition Metal-catalyzed Aromatic C-H Functionalization; 1.3.1.5 Other Methods 1.3.2 Diboronic Acids1.3.3 Heterocyclic Boronic Acids; 1.3.4 Alkenylboronic Acids; 1.3.4.1 Electrophilic Trapping of Alkenymetal Intermediates with Borates; 1.3.4.2 Transmetallation Methods; 1.3.4.3 Transition-metal Catalyzed Coupling between Alkenyl Halides/Triflates and Diboronyl Reagents; 1.3.4.4 Hydroboration of Alkynes; 1.3.4.5 Alkene Metathesis; 1.3.4.6 Other Methods; 1.3.5 Alkynylboronic Acids; 1.3.6 Alkylboronic Acids; 1.3.7 Allylic Boronic Acids; 1.3.8 Chemoselective Transformations of Compounds containing a Boronic Acid (Ester) Substituent; 1.3.8.1 Oxidative Methods 1.3.8.2 Reductive Methods1.3.8.3 Generation and Reactions of α-Boronyl-substituted Carbanions and Radicals; 1.3.8.4 Reactions of (α-Haloalkyl)boronic Esters; 1.3.8.5 Other Transformations; 1.4 Isolation and Characterization; 1.4.1 Chromatography and Recrystallization; 1.4.2 Solid Supports for Boronic Acid Immobilization and Purification; 1.4.2.1 Diethanolaminomethyl Polystyrene; 1.4.2.2 Other Solid-supported Diol Resins; 1.4.2.3 Soluble Diol Approaches; 1.4.3 Analytical and Spectroscopic Methods for Boronic Acid Derivatives; 1.4.3.1 Melting Points and Combustion Analysis 1.4.3.2 Mass Spectrometry1.4.3.3 Nuclear Magnetic Resonance Spectroscopy; 1.4.3.4 Other Spectroscopic Methods; 1.5 Overview of the Reactions of Boronic Acid Derivatives; 1.5.1 Metallation and Metal-catalyzed Protodeboronation; 1.5.2 Oxidative Replacement of Boron; 1.5.2.1 Oxygenation; 1.5.2.2 Amination; 1.5.2.3 Halogenation; 1.5.3 Carbon-Carbon Bond forming Processes; 1.5.3.1 Palladium-catalyzed Cross-coupling with Carbon Halides (Suzuki Coupling); 1.5.3.2 Allylation of Carbonyl Compounds; 1.5.3.3 Uncatalyzed Additions to Imines and Iminiums 1.5.3.4 Rhodium-catalyzed Additions to Aldehydes and Alkenes |
| Record Nr. | UNINA-9910144324903321 |
| Weinheim, : Wiley-VCH | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Boronic acids : preparation and applications in organic synthesis and medicine / / edited by Dennis G. Hall
| Boronic acids : preparation and applications in organic synthesis and medicine / / edited by Dennis G. Hall |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH |
| Descrizione fisica | 1 online resource (577 p.) |
| Disciplina | 547.05671 |
| Altri autori (Persone) | HallDennis |
| Soggetto topico |
Organic acids
Organoboron compounds Organic acids - Therapeutic use Organoboron compounds - Therapeutic use Organic acids - Synthesis Organoboron compounds - Synthesis |
| ISBN |
1-280-52116-3
9786610521166 3-527-60682-3 3-527-60654-8 1-60119-357-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Boronic Acids; Table of Contents; Preface; List of Authors; List of Abbreviations; 1 Structure, Properties, and Preparation Of Boronic Acid Derivatives. Overview of Their Reactions and Applications; 1.1 Introduction; 1.2 Structure and Properties of Boronic Acid Derivatives; 1.2.1 General Types and Nomenclature of Boronic Acid Derivatives; 1.2.2 Boronic Acids; 1.2.2.1 Structure and Bonding; 1.2.2.2 Physical Properties and Handling; 1.2.2.3 Safety Considerations; 1.2.2.4 Acidic Character; 1.2.2.5 Chemical Stability; 1.2.3 Boronic Acid Derivatives; 1.2.3.1 Boroxines; 1.2.3.2 Boronic Esters
1.2.3.3 Dialkoxyboranes and other Heterocyclic Boranes1.2.3.4 Diboronyl Esters; 1.2.3.5 Azaborolidines and other Boron Heterocycles; 1.2.3.6 Dihaloboranes and Monoalkylboranes; 1.2.3.7 Trifluoroborate Salts; 1.3 Synthesis of Boronic Acids and their Esters; 1.3.1 Arylboronic Acids; 1.3.1.1 Electrophilic Trapping of Arylmetal Intermediates with Borates; 1.3.1.2 Transmetallation of Aryl Silanes and Stannanes; 1.3.1.3 Coupling of Aryl Halides with Diboronyl Reagents; 1.3.1.4 Direct Boronylation by Transition Metal-catalyzed Aromatic C-H Functionalization; 1.3.1.5 Other Methods 1.3.2 Diboronic Acids1.3.3 Heterocyclic Boronic Acids; 1.3.4 Alkenylboronic Acids; 1.3.4.1 Electrophilic Trapping of Alkenymetal Intermediates with Borates; 1.3.4.2 Transmetallation Methods; 1.3.4.3 Transition-metal Catalyzed Coupling between Alkenyl Halides/Triflates and Diboronyl Reagents; 1.3.4.4 Hydroboration of Alkynes; 1.3.4.5 Alkene Metathesis; 1.3.4.6 Other Methods; 1.3.5 Alkynylboronic Acids; 1.3.6 Alkylboronic Acids; 1.3.7 Allylic Boronic Acids; 1.3.8 Chemoselective Transformations of Compounds containing a Boronic Acid (Ester) Substituent; 1.3.8.1 Oxidative Methods 1.3.8.2 Reductive Methods1.3.8.3 Generation and Reactions of α-Boronyl-substituted Carbanions and Radicals; 1.3.8.4 Reactions of (α-Haloalkyl)boronic Esters; 1.3.8.5 Other Transformations; 1.4 Isolation and Characterization; 1.4.1 Chromatography and Recrystallization; 1.4.2 Solid Supports for Boronic Acid Immobilization and Purification; 1.4.2.1 Diethanolaminomethyl Polystyrene; 1.4.2.2 Other Solid-supported Diol Resins; 1.4.2.3 Soluble Diol Approaches; 1.4.3 Analytical and Spectroscopic Methods for Boronic Acid Derivatives; 1.4.3.1 Melting Points and Combustion Analysis 1.4.3.2 Mass Spectrometry1.4.3.3 Nuclear Magnetic Resonance Spectroscopy; 1.4.3.4 Other Spectroscopic Methods; 1.5 Overview of the Reactions of Boronic Acid Derivatives; 1.5.1 Metallation and Metal-catalyzed Protodeboronation; 1.5.2 Oxidative Replacement of Boron; 1.5.2.1 Oxygenation; 1.5.2.2 Amination; 1.5.2.3 Halogenation; 1.5.3 Carbon-Carbon Bond forming Processes; 1.5.3.1 Palladium-catalyzed Cross-coupling with Carbon Halides (Suzuki Coupling); 1.5.3.2 Allylation of Carbonyl Compounds; 1.5.3.3 Uncatalyzed Additions to Imines and Iminiums 1.5.3.4 Rhodium-catalyzed Additions to Aldehydes and Alkenes |
| Record Nr. | UNINA-9911020126003321 |
| Weinheim, : Wiley-VCH | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Acid Derivatives, Supplement B, Part 1 . Volume 1
| The Chemistry of Acid Derivatives, Supplement B, Part 1 . Volume 1 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 |
| Descrizione fisica | 1 online resource (753 pages) : illustrations |
| Disciplina | 547.037 |
| Altri autori (Persone) | PataiSaul |
| Collana | Chemistry of functional groups |
| Soggetto topico |
Organic acids
Carboxylic acids |
| ISBN |
0-470-77849-0
0-470-77158-5 0-470-77188-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | V. 1. COOH, COOR, CONH₂ (2 v.) -- v. 2. COOH(R), CONH₂, COHal (2 v.). |
| Record Nr. | UNINA-9910830303003321 |
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Acid Derivatives, Supplement B, Part 1 . Volume 1
| The Chemistry of Acid Derivatives, Supplement B, Part 1 . Volume 1 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 |
| Descrizione fisica | 1 online resource (753 pages) : illustrations |
| Disciplina | 547.037 |
| Altri autori (Persone) | PataiSaul |
| Collana | Chemistry of functional groups |
| Soggetto topico |
Organic acids
Carboxylic acids |
| ISBN |
0-470-77849-0
0-470-77158-5 0-470-77188-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | V. 1. COOH, COOR, CONH₂ (2 v.) -- v. 2. COOH(R), CONH₂, COHal (2 v.). |
| Record Nr. | UNINA-9911019586903321 |
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Acid Derivatives, Supplement B, Part 2 . Volume 2
| The Chemistry of Acid Derivatives, Supplement B, Part 2 . Volume 2 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 |
| Descrizione fisica | 1 online resource (1473 pages) : illustrations |
| Disciplina | 547.037 |
| Altri autori (Persone) | PataiSaul |
| Collana | Chemistry of functional groups |
| Soggetto topico |
Organic acids
Carboxylic acids |
| ISBN |
0-470-77850-4
0-470-77159-3 0-470-77189-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | V. 1. COOH, COOR, CONH₂ (2 v.) -- v. 2. COOH(R), CONH₂, COHal (2 v.). |
| Record Nr. | UNINA-9910831081203321 |
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Acid Derivatives, Supplement B, Part 2 . Volume 2
| The Chemistry of Acid Derivatives, Supplement B, Part 2 . Volume 2 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 |
| Descrizione fisica | 1 online resource (1473 pages) : illustrations |
| Disciplina | 547.037 |
| Altri autori (Persone) | PataiSaul |
| Collana | Chemistry of functional groups |
| Soggetto topico |
Organic acids
Carboxylic acids |
| ISBN |
0-470-77850-4
0-470-77159-3 0-470-77189-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | V. 1. COOH, COOR, CONH₂ (2 v.) -- v. 2. COOH(R), CONH₂, COHal (2 v.). |
| Record Nr. | UNINA-9911020085203321 |
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1979 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Development of acid functional groups and lactones during the thermal degradation of wood and wood components [[electronic resource] /] / by David W. Rutherford, Robert L. Wershaw, and James B. Reeves III
| Development of acid functional groups and lactones during the thermal degradation of wood and wood components [[electronic resource] /] / by David W. Rutherford, Robert L. Wershaw, and James B. Reeves III |
| Autore | Rutherford David W |
| Edizione | [Version 1.0.] |
| Pubbl/distr/stampa | Reston, Va. : , : U.S. Geological Survey, , 2008 |
| Descrizione fisica | vi, 43 pages : digital, PDF file |
| Altri autori (Persone) |
WershawR. L
ReevesJames B |
| Collana | Scientific investigations report |
| Soggetto topico |
Wood - Deterioration
Charcoal Lactones Organic acids Fire |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910696550003321 |
Rutherford David W
|
||
| Reston, Va. : , : U.S. Geological Survey, , 2008 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||