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Annual reports on the progress of chemistry . Section C Physical chemistry
Annual reports on the progress of chemistry . Section C Physical chemistry
Pubbl/distr/stampa [London, England], : Royal Society of Chemistry, 1979-2013
Soggetto topico Chemistry, Inorganic
Chemistry, Organic
Chemistry, Physical and theoretical
Soggetto genere / forma Periodicals.
ISSN 1460-4787
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Annual reports on the progress of chemistry
Record Nr. UNISA-996212718903316
[London, England], : Royal Society of Chemistry, 1979-2013
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Annual reports on the progress of chemistry . Section C Physical chemistry
Annual reports on the progress of chemistry . Section C Physical chemistry
Pubbl/distr/stampa [London, England], : Royal Society of Chemistry, 1979-2013
Soggetto topico Chemistry, Inorganic
Chemistry, Organic
Chemistry, Physical and theoretical
Soggetto genere / forma Periodicals.
ISSN 1460-4787
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Annual reports on the progress of chemistry
Record Nr. UNINA-9910137803503321
[London, England], : Royal Society of Chemistry, 1979-2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Annual reports on the progress of chemistry . Section B Organic chemistry / / the Chemical Society
Annual reports on the progress of chemistry . Section B Organic chemistry / / the Chemical Society
Pubbl/distr/stampa London : , : The Chemical Society, , ©1968-[2013]
Descrizione fisica 1 online resource
Disciplina 547
Soggetto topico Chemistry, Organic
35.50 organic chemistry: general
Soggetto genere / forma Periodicals.
ISSN 1460-4779
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996214105303316
London : , : The Chemical Society, , ©1968-[2013]
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Annual reports on the progress of chemistry . Section B Organic chemistry / / the Chemical Society
Annual reports on the progress of chemistry . Section B Organic chemistry / / the Chemical Society
Pubbl/distr/stampa London : , : The Chemical Society, , ©1968-[2013]
Descrizione fisica 1 online resource
Disciplina 547
Soggetto topico Chemistry, Organic
35.50 organic chemistry: general
Soggetto genere / forma Periodicals.
ISSN 1460-4779
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910140926303321
London : , : The Chemical Society, , ©1968-[2013]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Annual reports online / / RSC
Annual reports online / / RSC
Pubbl/distr/stampa [London, England], : Royal Society of Chemistry
Soggetto topico Chemistry, Inorganic
Chemistry, Organic
Chemistry, Physical and theoretical
Soggetto genere / forma Periodicals.
ISSN 1460-4760
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Annual reports on the progress of chemistry
Record Nr. UNISA-996212719303316
[London, England], : Royal Society of Chemistry
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Annual reports online / / RSC
Annual reports online / / RSC
Pubbl/distr/stampa [London, England], : Royal Society of Chemistry
Soggetto topico Chemistry, Inorganic
Chemistry, Organic
Chemistry, Physical and theoretical
Soggetto genere / forma Periodicals.
ISSN 1460-4760
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Annual reports on the progress of chemistry
Record Nr. UNINA-9910140924503321
[London, England], : Royal Society of Chemistry
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Antimalarial Natural Products [[electronic resource] /] / edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M. Dirsch
Antimalarial Natural Products [[electronic resource] /] / edited by A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, Verena M. Dirsch
Edizione [1st ed. 2022.]
Pubbl/distr/stampa Cham : , : Springer International Publishing : , : Imprint : Springer, , 2022
Descrizione fisica 1 online resource (115 pages)
Disciplina 572
Collana Progress in the Chemistry of Organic Natural Products
Soggetto topico Natural products
Medicinal chemistry
Parasitology
Chemistry, Organic
Pharmaceutical chemistry
Natural Products
Medicinal Chemistry
Organic Chemistry
Pharmaceutics
ISBN 3-030-89873-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910733726203321
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Applications of dynamic NMR spectroscopy to organic chemistry / by Michinori Oki
Applications of dynamic NMR spectroscopy to organic chemistry / by Michinori Oki
Autore Oki, Michinori, 1928-
Pubbl/distr/stampa Deerfield Beach : VCH, c1985
Descrizione fisica xii, 423 p. : ill. ; 25 cm
Disciplina 547.128
Collana Methods in stereochemical analysis ; 4
Soggetto topico Nuclear magnetic resonance spectroscopy
Chemistry, Organic
ISBN 0895731207
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991004014439707536
Oki, Michinori, 1928-  
Deerfield Beach : VCH, c1985
Materiale a stampa
Lo trovi qui: Univ. del Salento
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Arene chemistry : reaction mechanisms and methods for aromatic compounds / / edited by Jacques Mortier
Arene chemistry : reaction mechanisms and methods for aromatic compounds / / edited by Jacques Mortier
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2016
Descrizione fisica 1 online resource (990 p.)
Disciplina 547/.61
Soggetto topico Aromatic compounds
Chemistry, Organic
ISBN 1-118-75498-0
1-118-75495-6
1-118-75488-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto TITLE PAGE ; COPYRIGHT PAGE ; CONTENTS; LIST OF CONTRIBUTORS; PREFACE; Part I Electrophilic Aromatic Substitution ; CHAPTER 1 ELECTROPHILIC AROMATIC SUBSTITUTION: MECHANISM ; 1.1 INTRODUCTION; 1.2 GENERAL ASPECTS; 1.3 ELECTROPHILES; 1.4 ARENE NUCLEOPHILES; 1.5 π-COMPLEX INTERMEDIATES ; 1.6 σ-COMPLEX OR WHELAND INTERMEDIATES ; 1.7 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 2 FRIEDEL-CRAFTS ALKYLATION OF ARENES IN TOTAL SYNTHESIS ; 2.1 INTRODUCTION; 2.2 TOTAL SYNTHESIS INVOLVING INTERMOLECULAR FC ALKYLATIONS; 2.2.1 Synthesis of Coenzyme Q10
2.2.2 Total Synthesis of (±)-Brasiliquinone B 2.2.3 Synthesis of (2212;)-Podophyllotoxin ; 2.2.4 Synthesis of Puupehenol and Related Compounds; 2.2.5 Synthesis of (2212;)-Talaumidin ; 2.2.6 Total Synthesis of (±)-Schefferine ; 2.3 TOTAL SYNTHESIS INVOLVING INTRAMOLECULAR FC ALKYLATIONS; 2.3.1 C-C Bond Formation Leading to Homocyclic Rings ; 2.3.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.3.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.4 TOTAL SYNTHESIS THROUGH TANDEM AND CASCADE PROCESSES INVOLVING FC REACTIONS
2.4.1 C-C Bond Formation Leading to Homocyclic Rings 2.4.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.4.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.5 TOTAL SYNTHESIS INVOLVING ipso-FC REACTIONS ; 2.5.1 Synthesis of (S)-(2212;)-Xylopinine ; 2.5.2 Synthesis of Garcibracteatone; 2.6 SUMMARY AND OUTLOOK; 2.7 ACKNOWLEDGMENT; ABBREVIATIONS ; REFERENCES; CHAPTER 3 CATALYTIC FRIEDEL-CRAFTS ACYLATION REACTIONS ; 3.1 INTRODUCTION AND HISTORICAL BACKGROUND; 3.2 CATALYTIC HOMOGENEOUS ACYLATIONS; 3.2.1 Metal Halides
3.2.2 Perfluoroalkanoic Acids, Perfluorosulfonic Acids, and Their (Metal) Derivatives 3.2.3 Miscellaneous; 3.3 CATALYTIC HETEROGENEOUS ACYLATIONS; 3.3.1 Zeolites; 3.3.2 Clays; 3.3.3 Metal Oxides; 3.3.4 Acid-Treated Metal Oxides ; 3.3.5 Heteropoly Acids (HPAs); 3.3.6 Nafion; 3.3.7 Miscellaneous; 3.4 DIRECT PHENOL ACYLATION; 3.5 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 4 THE USE OF QUANTUM CHEMISTRY FOR MECHANISTIC ANALYSES OF SEAr REACTIONS ; 4.1 INTRODUCTION; 4.1.1 Historical Overview of Early Quantum Chemistry Work
4.1.2 Current Mechanistic Understanding Based on Kinetic and Spectroscopic Studies 4.2 THE SEAr MECHANISM: QUANTUM CHEMICAL CHARACTERIZATION IN GAS PHASE AND SOLUTION; 4.2.1 Nitration and Nitrosation; 4.2.2 Halogenation; 4.2.3 Sulfonation; 4.2.4 Friedel-Crafts Alkylations and Acylations; 4.3 PREDICTION OF RELATIVE REACTIVITY AND REGIOSELECTIVITY BASED ON QUANTUM CHEMICAL DESCRIPTORS; 4.4 QUANTUM CHEMICAL REACTIVITY PREDICTION BASED ON MODELING OF TRANSITION STATES AND INTERMEDIATES; 4.4.1 Transition State Modeling; 4.4.2 The Reaction Intermediate or Sigma-Complex Approach
4.5 SUMMARY AND CONCLUSIONS
Record Nr. UNINA-9910137223403321
Hoboken, New Jersey : , : Wiley, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Arene chemistry : reaction mechanisms and methods for aromatic compounds / / edited by Jacques Mortier
Arene chemistry : reaction mechanisms and methods for aromatic compounds / / edited by Jacques Mortier
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2016
Descrizione fisica 1 online resource (990 p.)
Disciplina 547/.61
Soggetto topico Aromatic compounds
Chemistry, Organic
ISBN 1-118-75498-0
1-118-75495-6
1-118-75488-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto TITLE PAGE ; COPYRIGHT PAGE ; CONTENTS; LIST OF CONTRIBUTORS; PREFACE; Part I Electrophilic Aromatic Substitution ; CHAPTER 1 ELECTROPHILIC AROMATIC SUBSTITUTION: MECHANISM ; 1.1 INTRODUCTION; 1.2 GENERAL ASPECTS; 1.3 ELECTROPHILES; 1.4 ARENE NUCLEOPHILES; 1.5 π-COMPLEX INTERMEDIATES ; 1.6 σ-COMPLEX OR WHELAND INTERMEDIATES ; 1.7 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 2 FRIEDEL-CRAFTS ALKYLATION OF ARENES IN TOTAL SYNTHESIS ; 2.1 INTRODUCTION; 2.2 TOTAL SYNTHESIS INVOLVING INTERMOLECULAR FC ALKYLATIONS; 2.2.1 Synthesis of Coenzyme Q10
2.2.2 Total Synthesis of (±)-Brasiliquinone B 2.2.3 Synthesis of (2212;)-Podophyllotoxin ; 2.2.4 Synthesis of Puupehenol and Related Compounds; 2.2.5 Synthesis of (2212;)-Talaumidin ; 2.2.6 Total Synthesis of (±)-Schefferine ; 2.3 TOTAL SYNTHESIS INVOLVING INTRAMOLECULAR FC ALKYLATIONS; 2.3.1 C-C Bond Formation Leading to Homocyclic Rings ; 2.3.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.3.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.4 TOTAL SYNTHESIS THROUGH TANDEM AND CASCADE PROCESSES INVOLVING FC REACTIONS
2.4.1 C-C Bond Formation Leading to Homocyclic Rings 2.4.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.4.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.5 TOTAL SYNTHESIS INVOLVING ipso-FC REACTIONS ; 2.5.1 Synthesis of (S)-(2212;)-Xylopinine ; 2.5.2 Synthesis of Garcibracteatone; 2.6 SUMMARY AND OUTLOOK; 2.7 ACKNOWLEDGMENT; ABBREVIATIONS ; REFERENCES; CHAPTER 3 CATALYTIC FRIEDEL-CRAFTS ACYLATION REACTIONS ; 3.1 INTRODUCTION AND HISTORICAL BACKGROUND; 3.2 CATALYTIC HOMOGENEOUS ACYLATIONS; 3.2.1 Metal Halides
3.2.2 Perfluoroalkanoic Acids, Perfluorosulfonic Acids, and Their (Metal) Derivatives 3.2.3 Miscellaneous; 3.3 CATALYTIC HETEROGENEOUS ACYLATIONS; 3.3.1 Zeolites; 3.3.2 Clays; 3.3.3 Metal Oxides; 3.3.4 Acid-Treated Metal Oxides ; 3.3.5 Heteropoly Acids (HPAs); 3.3.6 Nafion; 3.3.7 Miscellaneous; 3.4 DIRECT PHENOL ACYLATION; 3.5 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 4 THE USE OF QUANTUM CHEMISTRY FOR MECHANISTIC ANALYSES OF SEAr REACTIONS ; 4.1 INTRODUCTION; 4.1.1 Historical Overview of Early Quantum Chemistry Work
4.1.2 Current Mechanistic Understanding Based on Kinetic and Spectroscopic Studies 4.2 THE SEAr MECHANISM: QUANTUM CHEMICAL CHARACTERIZATION IN GAS PHASE AND SOLUTION; 4.2.1 Nitration and Nitrosation; 4.2.2 Halogenation; 4.2.3 Sulfonation; 4.2.4 Friedel-Crafts Alkylations and Acylations; 4.3 PREDICTION OF RELATIVE REACTIVITY AND REGIOSELECTIVITY BASED ON QUANTUM CHEMICAL DESCRIPTORS; 4.4 QUANTUM CHEMICAL REACTIVITY PREDICTION BASED ON MODELING OF TRANSITION STATES AND INTERMEDIATES; 4.4.1 Transition State Modeling; 4.4.2 The Reaction Intermediate or Sigma-Complex Approach
4.5 SUMMARY AND CONCLUSIONS
Record Nr. UNINA-9910827921703321
Hoboken, New Jersey : , : Wiley, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui