top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.

Biblioteca

MARC Lista (tabellare)
Asymmetric synthesis in organophosphorus chemistry : synthetic methods, catalysis, and applications / / Oleg I. Kolodiazhnyi
Asymmetric synthesis in organophosphorus chemistry : synthetic methods, catalysis, and applications / / Oleg I. Kolodiazhnyi
Autore Kolodiazhnyi Oleg I.
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2017
Descrizione fisica 1 online resource (393 p.)
Disciplina 547.07
Soggetto topico Organophosphorus compounds
Asymmetric synthesis
ISBN 3-527-34153-6
3-527-34151-X
3-527-34154-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright; Dedication; Contents; Preface; Abbreviations; Chapter 1 Fundamentals of the Stereochemistry of Organophosphorus Compounds; 1.1 Historical Background; 1.2 Some Common Definitions in Stereochemistry; 1.3 Determination of Enantiomer Composition; 1.3.1 Method of Nuclear Magnetic Resonance; 1.3.1.1 Chiral Solvating Agents; 1.3.1.2 Complexes of Metals (Shift Reagents); 1.3.1.3 Chiral Derivatizing Agents for NMR; 1.3.2 Chromatographic Methods of Analysis; 1.3.2.1 Gas Chromatography; 1.3.2.2 Liquid Chromatography; 1.4 Determination of the Absolute Configuration
1.4.1 X-ray Crystal Analysis1.4.2 Method of Chemical Correlation; 1.4.3 The Assignment of Absolute Configuration by NMR; 1.5 Asymmetric Induction and Stereochemistry; 1.5.1 Asymmetric Induction; 1.5.2 Asymmetric Synthesis; 1.5.3 Asymmetric Transformation; 1.5.4 An Enantioselective Reaction; 1.5.5 Enantioselective Synthesis; 1.6 Summary; References; Chapter 2 Asymmetric Synthesis of P-Chirogenic Phosphorus Compounds; 2.1 Introduction; 2.2 Low-Coordinated Phosphorus Compounds; 2.3 Trivalent Tricoordinated Phosphorus Compounds; 2.3.1 Configuration Stability of P(III)-Compounds
2.3.2 Asymmetric Nucleophilic Substitution at P (III)2.3.2.1 Secondary Alcohols as Chiral Auxiliaries; 2.3.2.2 Optically Active Amines as Chiral Auxiliaries; 2.3.2.3 Ephedrine as Inductor of Chirality at P(III); 2.3.3 Asymmetric Oxidation of P(III) Compounds; 2.3.4 Asymmetric Electrophilic Substitution at P(III); 2.3.4.1 Asymmetric Michaelis-Arbuzov Reaction; 2.4 Pentavalent P(IV)-Phosphorus Compounds; 2.4.1 Introduction; 2.4.2 Nucleophilic Substitution Reactions; 2.4.2.1 Nucleophilic Substitution at P(IV) with Chiral Alcohol; 2.4.2.2 Nucleophilic Substitution at P(IV) with Chiral Amines
2.5 Chiral P(V) and P(VI) Phosphorus Compounds2.6 Summary; References; Chapter 3 Phosphorus Compounds with Chiral Side-Chain Centers; 3.1 Introduction; 3.2 Asymmetric Induction in Side Chains; 3.2.1 Transfer of Chirality from Phosphorus to Other Centers; 3.2.1.1 Chiral Phosphorus-Stabilized Anions; 3.2.1.2 1,2-Asymmetric Induction; 3.2.1.3 1,4-Asymmetric Induction; 3.3 Enantioselective Olefination; 3.4 Stereoselective Addition of Phosphorous Nucleophiles to C=X Bonds; 3.4.1 Phospha-Aldol Reaction; 3.4.2 Phospha-Mannich Reaction; 3.4.3 Phospha-Michael Reaction; 3.5 Asymmetric Reduction
3.6 Asymmetric Oxidation3.7 C-Modification; 3.8 Asymmetric Cycloaddition; 3.9 Multiple Stereoselectivity; 3.10 Summary; References; Chapter 4 Asymmetric Catalysis with Metal Complexes; 4.1 Introduction; 4.2 Asymmetric Catalytic Hydrogenation and Other Reactions of Reduction; 4.2.1 Hydrogenation of C=C Phosphorus Compounds; 4.2.2 Hydrogenation of C=O Phosphorus Compounds; 4.3 Asymmetric Reduction and Oxidation; 4.3.1 Reduction of C=O, C=N, and C=C bonds; 4.3.2 Asymmetric Oxidation; 4.4 Electrophilic Asymmetric Catalysis; 4.4.1 Catalytic Electrophilic Substitution at the Phosphorus Atom
4.4.1.1 Alkylation and Arylation of P(III) Compounds
Record Nr. UNINA-9910134858903321
Kolodiazhnyi Oleg I.  
Weinheim, Germany : , : Wiley-VCH, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Asymmetric synthesis in organophosphorus chemistry : synthetic methods, catalysis, and applications / / Oleg I. Kolodiazhnyi
Asymmetric synthesis in organophosphorus chemistry : synthetic methods, catalysis, and applications / / Oleg I. Kolodiazhnyi
Autore Kolodiazhnyi Oleg I.
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2017
Descrizione fisica 1 online resource (393 p.)
Disciplina 547.07
Soggetto topico Organophosphorus compounds
Asymmetric synthesis
ISBN 3-527-34153-6
3-527-34151-X
3-527-34154-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Title Page; Copyright; Dedication; Contents; Preface; Abbreviations; Chapter 1 Fundamentals of the Stereochemistry of Organophosphorus Compounds; 1.1 Historical Background; 1.2 Some Common Definitions in Stereochemistry; 1.3 Determination of Enantiomer Composition; 1.3.1 Method of Nuclear Magnetic Resonance; 1.3.1.1 Chiral Solvating Agents; 1.3.1.2 Complexes of Metals (Shift Reagents); 1.3.1.3 Chiral Derivatizing Agents for NMR; 1.3.2 Chromatographic Methods of Analysis; 1.3.2.1 Gas Chromatography; 1.3.2.2 Liquid Chromatography; 1.4 Determination of the Absolute Configuration
1.4.1 X-ray Crystal Analysis1.4.2 Method of Chemical Correlation; 1.4.3 The Assignment of Absolute Configuration by NMR; 1.5 Asymmetric Induction and Stereochemistry; 1.5.1 Asymmetric Induction; 1.5.2 Asymmetric Synthesis; 1.5.3 Asymmetric Transformation; 1.5.4 An Enantioselective Reaction; 1.5.5 Enantioselective Synthesis; 1.6 Summary; References; Chapter 2 Asymmetric Synthesis of P-Chirogenic Phosphorus Compounds; 2.1 Introduction; 2.2 Low-Coordinated Phosphorus Compounds; 2.3 Trivalent Tricoordinated Phosphorus Compounds; 2.3.1 Configuration Stability of P(III)-Compounds
2.3.2 Asymmetric Nucleophilic Substitution at P (III)2.3.2.1 Secondary Alcohols as Chiral Auxiliaries; 2.3.2.2 Optically Active Amines as Chiral Auxiliaries; 2.3.2.3 Ephedrine as Inductor of Chirality at P(III); 2.3.3 Asymmetric Oxidation of P(III) Compounds; 2.3.4 Asymmetric Electrophilic Substitution at P(III); 2.3.4.1 Asymmetric Michaelis-Arbuzov Reaction; 2.4 Pentavalent P(IV)-Phosphorus Compounds; 2.4.1 Introduction; 2.4.2 Nucleophilic Substitution Reactions; 2.4.2.1 Nucleophilic Substitution at P(IV) with Chiral Alcohol; 2.4.2.2 Nucleophilic Substitution at P(IV) with Chiral Amines
2.5 Chiral P(V) and P(VI) Phosphorus Compounds2.6 Summary; References; Chapter 3 Phosphorus Compounds with Chiral Side-Chain Centers; 3.1 Introduction; 3.2 Asymmetric Induction in Side Chains; 3.2.1 Transfer of Chirality from Phosphorus to Other Centers; 3.2.1.1 Chiral Phosphorus-Stabilized Anions; 3.2.1.2 1,2-Asymmetric Induction; 3.2.1.3 1,4-Asymmetric Induction; 3.3 Enantioselective Olefination; 3.4 Stereoselective Addition of Phosphorous Nucleophiles to C=X Bonds; 3.4.1 Phospha-Aldol Reaction; 3.4.2 Phospha-Mannich Reaction; 3.4.3 Phospha-Michael Reaction; 3.5 Asymmetric Reduction
3.6 Asymmetric Oxidation3.7 C-Modification; 3.8 Asymmetric Cycloaddition; 3.9 Multiple Stereoselectivity; 3.10 Summary; References; Chapter 4 Asymmetric Catalysis with Metal Complexes; 4.1 Introduction; 4.2 Asymmetric Catalytic Hydrogenation and Other Reactions of Reduction; 4.2.1 Hydrogenation of C=C Phosphorus Compounds; 4.2.2 Hydrogenation of C=O Phosphorus Compounds; 4.3 Asymmetric Reduction and Oxidation; 4.3.1 Reduction of C=O, C=N, and C=C bonds; 4.3.2 Asymmetric Oxidation; 4.4 Electrophilic Asymmetric Catalysis; 4.4.1 Catalytic Electrophilic Substitution at the Phosphorus Atom
4.4.1.1 Alkylation and Arylation of P(III) Compounds
Record Nr. UNINA-9910814764703321
Kolodiazhnyi Oleg I.  
Weinheim, Germany : , : Wiley-VCH, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Autore Timperley Christopher M.
Pubbl/distr/stampa London, England : , : Academic Press, , 2015
Descrizione fisica 1 online resource (787 p.)
Disciplina 547.07
Collana Best Synthetic Methods
Soggetto topico Organophosphorus compounds
Soggetto genere / forma Electronic books.
ISBN 0-08-101580-1
0-08-098224-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Best Synthetic Methods; OTHER VOLUMES IN THE SERIES; Best Synthetic Methods; Copyright; ACKNOWLEDGEMENTS; REFERENCES; 1.4 PHOSPHORUS COMPOUNDS IN LIVING SYSTEMS; 1.5.3 ORGANOPHOSPHORUS PESTICIDES; 1.6 NOMENCLATURE OF ORGANOPHOSPHORUS COMPOUNDS; 1.7 CHIRAL PHOSPHORUS COMPOUNDS AND BIOLOGICAL IMPLICATIONS; 1.8 PHOSPHORUS-CONTAINING PHARMACEUTICALS; 1.9 FIRE RETARDANTS AND FIRE-EXTINGUISHING COMPOUNDS; 1.10 TOXICOLOGY AND MEDICAL TREATMENT OF ORGANOPHOSPHORUS COMPOUNDS; 1.11 FLUOROGENIC NERVE AGENT MIMICS FOR SCREENING FOR IMPROVED BIOSCAVENGERS
4.48 DIALKYL N-HYDROXY/ALKOXYPHOSPHORAMIDATES (RO)2P(O)NHOR (R=H OR ALKYL)
Record Nr. UNINA-9910459089603321
Timperley Christopher M.  
London, England : , : Academic Press, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Autore Timperley Christopher M.
Pubbl/distr/stampa London, England : , : Academic Press, , 2015
Descrizione fisica 1 online resource (787 p.)
Disciplina 547.07
Collana Best Synthetic Methods
Soggetto topico Organophosphorus compounds
ISBN 0-08-101580-1
0-08-098224-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Best Synthetic Methods; OTHER VOLUMES IN THE SERIES; Best Synthetic Methods; Copyright; ACKNOWLEDGEMENTS; REFERENCES; 1.4 PHOSPHORUS COMPOUNDS IN LIVING SYSTEMS; 1.5.3 ORGANOPHOSPHORUS PESTICIDES; 1.6 NOMENCLATURE OF ORGANOPHOSPHORUS COMPOUNDS; 1.7 CHIRAL PHOSPHORUS COMPOUNDS AND BIOLOGICAL IMPLICATIONS; 1.8 PHOSPHORUS-CONTAINING PHARMACEUTICALS; 1.9 FIRE RETARDANTS AND FIRE-EXTINGUISHING COMPOUNDS; 1.10 TOXICOLOGY AND MEDICAL TREATMENT OF ORGANOPHOSPHORUS COMPOUNDS; 1.11 FLUOROGENIC NERVE AGENT MIMICS FOR SCREENING FOR IMPROVED BIOSCAVENGERS
4.48 DIALKYL N-HYDROXY/ALKOXYPHOSPHORAMIDATES (RO)2P(O)NHOR (R=H OR ALKYL)
Record Nr. UNINA-9910792482903321
Timperley Christopher M.  
London, England : , : Academic Press, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Best synthetic methods : organophosphorus (V) chemistry / / co-authored and edited by Christopher M. Timperley ; contributors, Nicholas Cooper [and seven others]
Autore Timperley Christopher M.
Pubbl/distr/stampa London, England : , : Academic Press, , 2015
Descrizione fisica 1 online resource (787 p.)
Disciplina 547.07
Collana Best Synthetic Methods
Soggetto topico Organophosphorus compounds
ISBN 0-08-101580-1
0-08-098224-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Best Synthetic Methods; OTHER VOLUMES IN THE SERIES; Best Synthetic Methods; Copyright; ACKNOWLEDGEMENTS; REFERENCES; 1.4 PHOSPHORUS COMPOUNDS IN LIVING SYSTEMS; 1.5.3 ORGANOPHOSPHORUS PESTICIDES; 1.6 NOMENCLATURE OF ORGANOPHOSPHORUS COMPOUNDS; 1.7 CHIRAL PHOSPHORUS COMPOUNDS AND BIOLOGICAL IMPLICATIONS; 1.8 PHOSPHORUS-CONTAINING PHARMACEUTICALS; 1.9 FIRE RETARDANTS AND FIRE-EXTINGUISHING COMPOUNDS; 1.10 TOXICOLOGY AND MEDICAL TREATMENT OF ORGANOPHOSPHORUS COMPOUNDS; 1.11 FLUOROGENIC NERVE AGENT MIMICS FOR SCREENING FOR IMPROVED BIOSCAVENGERS
4.48 DIALKYL N-HYDROXY/ALKOXYPHOSPHORAMIDATES (RO)2P(O)NHOR (R=H OR ALKYL)
Record Nr. UNINA-9910815455603321
Timperley Christopher M.  
London, England : , : Academic Press, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The Chemistry of Organophosphorous Compounds, Phosphine Oxides, Sulphides, Selenides and Tellurides. Vol. 2
The Chemistry of Organophosphorous Compounds, Phosphine Oxides, Sulphides, Selenides and Tellurides. Vol. 2
Autore Hartley Frank R
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Incorporated, 1992
Descrizione fisica 1 online resource (xvi, 647 pages) : illustrations
Disciplina 547.070459
Altri autori (Persone) HartleyF. R
Collana PATAI'S Chemistry of Functional Groups
Soggetto topico Organophosphorus compounds
ISBN 0-470-77903-9
0-470-03442-4
0-470-02772-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Structure and bonding in tertiary phosphine chalcogenides / D.G. Gilheany -- Structure and stereochemistry of secondary and tertiary phosphine chalcogenides / M.J. Gallagher -- Electrochemistry of organophosphorus(V) compounds / K.S.V. Santhanam -- Photochemistry of phosphine chalcogenides / M. Dankowski -- Spectroscopy of phosphine chalcogenides / G. Davidson -- Methods of preparation of phosphine chalcogenides / A.K. Bhattacharya and N.K. Roy -- Chemical properties and reactions of phosphine chalcogenides / R.S. Edmundson -- Coordination chemistry of phosphine chalcogenides and their analytical and catalytic applications / T.S. Lobana.
Record Nr. UNINA-9910830100703321
Hartley Frank R  
[Place of publication not identified], : John Wiley & Sons Incorporated, 1992
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The Chemistry of Organophosphorous Compounds. Vol. 1
The Chemistry of Organophosphorous Compounds. Vol. 1
Autore Hartley Frank R
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Incorporated, 1990
Descrizione fisica 1 online resource (xiv, 739 pages) : illustrations
Disciplina 547.070459
Altri autori (Persone) HartleyF. R
Collana PATAI'S Chemistry of Functional Groups
Soggetto topico Organophosphorus compounds
ISBN 0-470-77894-6
0-470-03443-2
0-470-02770-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto V. 1. Primary, secondary, and tertiary phosphines, polyphosphines, and heterocyclic organophosphorus (III) compounds -- v. 2. Phosphine oxides, sulphides, selenides and tellurides -- v. 3. Phosphonium salts, ylides and phosphoranes.
Record Nr. UNINA-9910829945603321
Hartley Frank R  
[Place of publication not identified], : John Wiley & Sons Incorporated, 1990
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The Chemistry of Organophosphorus Compounds, Phosphonium Salts, Ylides and Phosphoranes. Vol. 3, Phosphonium Salts, Ylides and Phosphoranes
The Chemistry of Organophosphorus Compounds, Phosphonium Salts, Ylides and Phosphoranes. Vol. 3, Phosphonium Salts, Ylides and Phosphoranes
Autore Hartley Frank R
Pubbl/distr/stampa [Place of publication not identified], : John Wiley & Sons Incorporated, 1994
Descrizione fisica 1 online resource (442 pages) : illustrations
Disciplina 547.07
Altri autori (Persone) HartleyF. R
Collana Chemistry of functional groups
Soggetto topico Organophosphorus compounds
ISBN 0-470-77908-X
0-470-02773-8
0-470-03436-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Structure and bonding in phosphonium ylides, salts and phosphoranes -- D.G. Gilheany -- Preparation, properties and reactions of phosphonium salts -- H.-J. Cristau and F. Plénat -- Preparation, properties and reactions of phosphoranes -- Ramon Burgada and Ralph Setton -- Structure, bonding and spectroscopic properties of phosphonium ylides -- S.M. Bachrach and C.I. Nitsche -- Electrochemistry of ylides, phosphoranes and phosphonium salts -- K.S.V. Santhanam -- Photochemistry of phosphonium salts, phosphoranes and ylides -- M. Dankowski -- Chemical analysis of organophosphorus compounds -- H. Feilchenfeld.
Record Nr. UNINA-9910830108503321
Hartley Frank R  
[Place of publication not identified], : John Wiley & Sons Incorporated, 1994
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The heterocyclic derivatives of phosphorus, arsenic, antimony, and bismuth [[electronic resource]]
The heterocyclic derivatives of phosphorus, arsenic, antimony, and bismuth [[electronic resource]]
Autore Mann Frederick George
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Wiley-Interscience, 1970
Descrizione fisica 1 online resource (743 p.)
Disciplina 547.59
547/.59
547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Organophosphorus compounds
Organoarsenic compounds
Organoantimony compounds
Organobismuth compounds
ISBN 1-282-30135-7
9786612301353
0-470-18650-X
0-470-18800-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Heterocyclic Derivatives of PHOSPHORUS, ARSENIC, ANTIMONY and BISMUTH; Introduction to the Series; Preface; Note on Nomenclature; Contents; Part I. Heterocyclic Derivatives of Phosphorus; Phosphorus only; 1P; Three-membered Ring Systems; 1H-Phosphirene and Phosphirane; Four-membered Ring Systems; Phosphetes, Phosphetenes, and Phosphetanes; Five-membered Ring Systems; Phospholes, Phospholenes, and Phospholanes; Phospholes; Phospholenes; Phospholanes; 5-Phosphoniaspiro[4.4]nonane Cation; 5-Phospha(v)spiro[4.4]nonane; Phosphmdole and Phosphindolines; Isophosphindole and Isophosphindolines
5H-Dibenzophosphole (9-Phoaphafluomne)Phosphoranes containing Dibenzophosphole Units; Tris-(2,2'-biphenylylene)phosphate Anion; Six-membered Ring Systems; Phosphorin and Phoaphorinanes; 5-Phosphoniaspiro[4.5]decme Cation; 6-Phosphoniaspiro[5.5]undecane Cation; 1H-Phosphorinof4,3-b]indole; Phosphorino[4,3-b]quinoline; Phosphinoline and Tetrahydrophosphinolinos; 1,1'( 2H,2'H)-Spirobiphosphinolinium Cation; 5H-Phosphinolino[4,3-b]indole; Phosphinolino[4,3-b]quinolines; Isophosphinoline and Tetrahydroisophosphinolines; Dibenzo[b,e]phosphorin; Dibenzo[b,d]phosphorin; Seven-membered ring Systems
1H-Phosphepin and Phosphepanes5H-Dibenzo[b,f]phosphepin; Eight-membered Ring System; 8-Phosphatetracyclo[2.2.1.12,6.03,5]octane; Nine-membered Ring Systems; Phosphonin and Phosphonanes; 17H-Tetrabenzo[b.d,f,h]phosphonin and 17H-Triberizo[b,d,f]naphtho-[1,2-h]phosphonin; 9-Phosphabicyclo[6.1.0]nona-2,4,6-triene; 9-Phosphabicyclo[4.2.1]nona-2,4,7-triene; 2P; Four-membered Ring Systems; 1,2-Diphosphete, 1,2-Diphosphetins, and 1,2-Diphosphetane; Five-membered Ring Systems; Diphoepholes and Diphospholanea; 1,2-Diphospholanes; 1,3-Diphospholanes; Six-membered Ring Systems
Diphosphorins and Diphosphorinanes1,2-Diphosphorin and 1,2-Diphosphorinanes; 1,3-Diphosphorin and 1,3-Diphoaphorinanes; 1,3-Benzodiphoaphorin; 1,4-Diphosphorin and 1,4-Diphosphorinanes; 1,4-Diphosphabicyclo[2.2.2]octane; 1,4-Benzodiphosphorin; Phosphanthrene; 5,10-Ethanophosphanthrene; 5,12-o-Benzenodibemo[b,f] [1,4]diphosphocin; Seven-membered Ring System; 5H-Dibenzo[d,f][1,3]diphosphepin; Eight-membered Ring Systems; 1,5-Diphosphocin and 1,5-Diphosphocane; 2,5-Benzodiphosphocin; Dibenzo[e,g][ 1,4]diphosphocin; Dibenzo[b,f] [1,5]diphoephocin; Nine-membered Ring System
5H-Dibenzo[f,h] [1,5]diphosphoninTen-membered Ring Systems; Dibenzo[b,d][1,6]diphosphecin arid Tribeiiao[b,d,h] [1,6]diphosphecin; 3P; Five-membered Ring Systems; 1H-1,2,3-Triphosphole; 1H- 1,2,3-Banzotriphoapholo; 4P; Eight-membered Ring System; 1,3,5,7 -Tetraphosphocin; Phosphorus and Nitrogen; Four-membered Ring System; 1P + 2N; 1,3,2-Diazaphosphete and 1,3,2-Diazaphosphetidines; Five-membered Ring Systems; 1P + 1N; 1H-1,2-Azaphosphole and 1,2-Azaphospholidine; 1H -1,3-Azaphosphole and 1,3-Azaphospholidine-2-spirocyclopentane; 1P + 2N; 4H- 1,2,4-Diazaphosphole
1H- 1,4,2-Diazaphosphole and 1,4,2-Diazaphospholidincs
Record Nr. UNINA-9910144290403321
Mann Frederick George  
New York, : Wiley-Interscience, 1970
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The heterocyclic derivatives of phosphorus, arsenic, antimony, and bismuth [[electronic resource]]
The heterocyclic derivatives of phosphorus, arsenic, antimony, and bismuth [[electronic resource]]
Autore Mann Frederick George
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Wiley-Interscience, 1970
Descrizione fisica 1 online resource (743 p.)
Disciplina 547.59
547/.59
547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Organophosphorus compounds
Organoarsenic compounds
Organoantimony compounds
Organobismuth compounds
ISBN 1-282-30135-7
9786612301353
0-470-18650-X
0-470-18800-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto The Heterocyclic Derivatives of PHOSPHORUS, ARSENIC, ANTIMONY and BISMUTH; Introduction to the Series; Preface; Note on Nomenclature; Contents; Part I. Heterocyclic Derivatives of Phosphorus; Phosphorus only; 1P; Three-membered Ring Systems; 1H-Phosphirene and Phosphirane; Four-membered Ring Systems; Phosphetes, Phosphetenes, and Phosphetanes; Five-membered Ring Systems; Phospholes, Phospholenes, and Phospholanes; Phospholes; Phospholenes; Phospholanes; 5-Phosphoniaspiro[4.4]nonane Cation; 5-Phospha(v)spiro[4.4]nonane; Phosphmdole and Phosphindolines; Isophosphindole and Isophosphindolines
5H-Dibenzophosphole (9-Phoaphafluomne)Phosphoranes containing Dibenzophosphole Units; Tris-(2,2'-biphenylylene)phosphate Anion; Six-membered Ring Systems; Phosphorin and Phoaphorinanes; 5-Phosphoniaspiro[4.5]decme Cation; 6-Phosphoniaspiro[5.5]undecane Cation; 1H-Phosphorinof4,3-b]indole; Phosphorino[4,3-b]quinoline; Phosphinoline and Tetrahydrophosphinolinos; 1,1'( 2H,2'H)-Spirobiphosphinolinium Cation; 5H-Phosphinolino[4,3-b]indole; Phosphinolino[4,3-b]quinolines; Isophosphinoline and Tetrahydroisophosphinolines; Dibenzo[b,e]phosphorin; Dibenzo[b,d]phosphorin; Seven-membered ring Systems
1H-Phosphepin and Phosphepanes5H-Dibenzo[b,f]phosphepin; Eight-membered Ring System; 8-Phosphatetracyclo[2.2.1.12,6.03,5]octane; Nine-membered Ring Systems; Phosphonin and Phosphonanes; 17H-Tetrabenzo[b.d,f,h]phosphonin and 17H-Triberizo[b,d,f]naphtho-[1,2-h]phosphonin; 9-Phosphabicyclo[6.1.0]nona-2,4,6-triene; 9-Phosphabicyclo[4.2.1]nona-2,4,7-triene; 2P; Four-membered Ring Systems; 1,2-Diphosphete, 1,2-Diphosphetins, and 1,2-Diphosphetane; Five-membered Ring Systems; Diphoepholes and Diphospholanea; 1,2-Diphospholanes; 1,3-Diphospholanes; Six-membered Ring Systems
Diphosphorins and Diphosphorinanes1,2-Diphosphorin and 1,2-Diphosphorinanes; 1,3-Diphosphorin and 1,3-Diphoaphorinanes; 1,3-Benzodiphoaphorin; 1,4-Diphosphorin and 1,4-Diphosphorinanes; 1,4-Diphosphabicyclo[2.2.2]octane; 1,4-Benzodiphosphorin; Phosphanthrene; 5,10-Ethanophosphanthrene; 5,12-o-Benzenodibemo[b,f] [1,4]diphosphocin; Seven-membered Ring System; 5H-Dibenzo[d,f][1,3]diphosphepin; Eight-membered Ring Systems; 1,5-Diphosphocin and 1,5-Diphosphocane; 2,5-Benzodiphosphocin; Dibenzo[e,g][ 1,4]diphosphocin; Dibenzo[b,f] [1,5]diphoephocin; Nine-membered Ring System
5H-Dibenzo[f,h] [1,5]diphosphoninTen-membered Ring Systems; Dibenzo[b,d][1,6]diphosphecin arid Tribeiiao[b,d,h] [1,6]diphosphecin; 3P; Five-membered Ring Systems; 1H-1,2,3-Triphosphole; 1H- 1,2,3-Banzotriphoapholo; 4P; Eight-membered Ring System; 1,3,5,7 -Tetraphosphocin; Phosphorus and Nitrogen; Four-membered Ring System; 1P + 2N; 1,3,2-Diazaphosphete and 1,3,2-Diazaphosphetidines; Five-membered Ring Systems; 1P + 1N; 1H-1,2-Azaphosphole and 1,2-Azaphospholidine; 1H -1,3-Azaphosphole and 1,3-Azaphospholidine-2-spirocyclopentane; 1P + 2N; 4H- 1,2,4-Diazaphosphole
1H- 1,4,2-Diazaphosphole and 1,4,2-Diazaphospholidincs
Record Nr. UNINA-9910830432403321
Mann Frederick George  
New York, : Wiley-Interscience, 1970
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui