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MARC Lista (tabellare)
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
Autore Maretina Irina A
Pubbl/distr/stampa Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014
Descrizione fisica 1 online resource (312 p.)
Disciplina 547/.413
Altri autori (Persone) TebbyJohn C. <1933->
IoninB. I
Soggetto topico Alkynes
Ring formation (Chemistry)
ISBN 1-118-70929-2
1-118-70931-4
1-118-70933-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Alkynes in Cycloadditions; Contents; Preface; Acknowledgments; Biography; 1 Introduction; 2 Regioselective Syntheses of Polysubstituted Benzenes Catalyzed by Transition Metal Complexes; 2.1 [2+2+2] Cycloaddition Reactions of Acetylenes; 2.1.1 Reactions of Alkynes with Metallocyclopentadiene as an Intermediate; 2.1.2 Intra-intermolecular [2+2+2] Cycloaddition of Alkynes; 2.2 Stereochemical Aspect of Intramolecular and Intermolecular Reactions of Diynes with Monoalkynes; 2.2.1 Strategy of Enantioselective [2+2+2] Cycloaddition; 2.3 Heteroatom Bound to the Triple Bond
2.3.1 Nitrogen-Containing Substrates2.3.2 [2+2+2] Cycloadditions of Alkynes to Nitriles: Synthesis of Pyridines; 2.4 Heterohelicens. Asymmetric Syntheses; 2.4.1 Oxygen-Containing Helicens; 2.4.2 Nitrogen-Containing Helicens. Helical Dications; 2.5 Aromatic Rings with Boron and Silicon Substituents; 2.6 [2+2+2] Cycloaddition Reactions of 1-Alkynylphosphines and Their Derivatives; 2.7 Intramolecular [2+2+2] Cycloaddition of Diynes to Alkenes; 2.7.1 Allene as an Alkene Component; 2.7.2 Formation of Polycyclic Cyclohexadienes by Ru-catalyzed Cascade Reactions of 1,6-Diynes and Alkenes
2.7.3 Stereochemical Aspects of the Reaction of Diynes with Alkenes2.7.4 Hetero-[2+2+2] Cycloaddition of Alkynes to Compounds with a Multiple Carbon-Heteroatom Bond; 2.8 Reactions of [4+2] Cycloaddition and Other Approaches to the Synthesis of Polysubstituted Benzenes; 2.8.1 Reactions of Conjugated Enynes; 2.8.2 Acceleration of Pd-catalyzed [4+2]-Benzannulation in the Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bronsted Bases; 2.9 Combined Reactions
2.9.1 Formal [4+2+2] Cycloaddition of 1,6-Diynes to 1,3-Dienes Catalyzed by Ru: Formation of Cyclooctatrienes and Vinylcyclohexadienes2.9.2 Formation of Eight-Membered Ring Systems by [4+2+2] Annulation; 2.9.3 AuBr3 (AlCl3)- and Cu(OTf)2-Catalyzed [4+2] Cycloaddition of Alkynyl- and Alkenyl-Enynones and Enynals: An Approach to Functionalized Polycyclic Hydrocarbons; 2.10 Construction of Polycyclic Systems; 2.10.1 Strategies for the Synthesis of Steroid Systems by Co-catalyzed [2+2+2] Cycloaddition of Nonconjugated Enyne-Allenes and Enediynes
2.10.2 Cobalt(I)-Mediated [2+2+2] Cyclization of Allene-Diynes: A Diastereoselective Approach to 11-aryl Steroid Core. 11-Aryl-Substituted Steroid Systems by Co-catalyzed [2+2+2] Cyclization of Allene-Diynes2.10.3 Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via Intramolecular Cobalt-Mediated [2+2+2] Cycloaddition; 2.10.4 Intramolecular Cycloaddition of Nonconjugated Enediynes of a Higher Order as a Route to Functionalized Condensed Polycyclic Systems; 2.10.5 A Strategy for the Synthesis of Aromatic Molecular-Bowl Hydrocarbons
2.10.6 A Route to Archimedenes: Total Synthesis of C3h-symmetric [7]phenylenes
Record Nr. UNINA-9910138996803321
Maretina Irina A  
Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
Autore Maretina Irina A
Pubbl/distr/stampa Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014
Descrizione fisica 1 online resource (312 p.)
Disciplina 547/.413
Altri autori (Persone) TebbyJohn C. <1933->
IoninB. I
Soggetto topico Alkynes
Ring formation (Chemistry)
ISBN 1-118-70929-2
1-118-70931-4
1-118-70933-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Alkynes in Cycloadditions; Contents; Preface; Acknowledgments; Biography; 1 Introduction; 2 Regioselective Syntheses of Polysubstituted Benzenes Catalyzed by Transition Metal Complexes; 2.1 [2+2+2] Cycloaddition Reactions of Acetylenes; 2.1.1 Reactions of Alkynes with Metallocyclopentadiene as an Intermediate; 2.1.2 Intra-intermolecular [2+2+2] Cycloaddition of Alkynes; 2.2 Stereochemical Aspect of Intramolecular and Intermolecular Reactions of Diynes with Monoalkynes; 2.2.1 Strategy of Enantioselective [2+2+2] Cycloaddition; 2.3 Heteroatom Bound to the Triple Bond
2.3.1 Nitrogen-Containing Substrates2.3.2 [2+2+2] Cycloadditions of Alkynes to Nitriles: Synthesis of Pyridines; 2.4 Heterohelicens. Asymmetric Syntheses; 2.4.1 Oxygen-Containing Helicens; 2.4.2 Nitrogen-Containing Helicens. Helical Dications; 2.5 Aromatic Rings with Boron and Silicon Substituents; 2.6 [2+2+2] Cycloaddition Reactions of 1-Alkynylphosphines and Their Derivatives; 2.7 Intramolecular [2+2+2] Cycloaddition of Diynes to Alkenes; 2.7.1 Allene as an Alkene Component; 2.7.2 Formation of Polycyclic Cyclohexadienes by Ru-catalyzed Cascade Reactions of 1,6-Diynes and Alkenes
2.7.3 Stereochemical Aspects of the Reaction of Diynes with Alkenes2.7.4 Hetero-[2+2+2] Cycloaddition of Alkynes to Compounds with a Multiple Carbon-Heteroatom Bond; 2.8 Reactions of [4+2] Cycloaddition and Other Approaches to the Synthesis of Polysubstituted Benzenes; 2.8.1 Reactions of Conjugated Enynes; 2.8.2 Acceleration of Pd-catalyzed [4+2]-Benzannulation in the Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bronsted Bases; 2.9 Combined Reactions
2.9.1 Formal [4+2+2] Cycloaddition of 1,6-Diynes to 1,3-Dienes Catalyzed by Ru: Formation of Cyclooctatrienes and Vinylcyclohexadienes2.9.2 Formation of Eight-Membered Ring Systems by [4+2+2] Annulation; 2.9.3 AuBr3 (AlCl3)- and Cu(OTf)2-Catalyzed [4+2] Cycloaddition of Alkynyl- and Alkenyl-Enynones and Enynals: An Approach to Functionalized Polycyclic Hydrocarbons; 2.10 Construction of Polycyclic Systems; 2.10.1 Strategies for the Synthesis of Steroid Systems by Co-catalyzed [2+2+2] Cycloaddition of Nonconjugated Enyne-Allenes and Enediynes
2.10.2 Cobalt(I)-Mediated [2+2+2] Cyclization of Allene-Diynes: A Diastereoselective Approach to 11-aryl Steroid Core. 11-Aryl-Substituted Steroid Systems by Co-catalyzed [2+2+2] Cyclization of Allene-Diynes2.10.3 Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via Intramolecular Cobalt-Mediated [2+2+2] Cycloaddition; 2.10.4 Intramolecular Cycloaddition of Nonconjugated Enediynes of a Higher Order as a Route to Functionalized Condensed Polycyclic Systems; 2.10.5 A Strategy for the Synthesis of Aromatic Molecular-Bowl Hydrocarbons
2.10.6 A Route to Archimedenes: Total Synthesis of C3h-symmetric [7]phenylenes
Record Nr. UNINA-9910826821803321
Maretina Irina A  
Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral auxiliaries in cycloadditions / / Karola Ruck-Braun, Horst Kunz
Chiral auxiliaries in cycloadditions / / Karola Ruck-Braun, Horst Kunz
Autore Rück-Braun Karola
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH, , 1999
Descrizione fisica 1 online resource (190 p.)
Disciplina 547.2
547.504593
Soggetto topico Chirality
Ring formation (Chemistry)
Organic compounds - Synthesis
Soggetto genere / forma Electronic books.
ISBN 1-281-84251-6
9786611842512
3-527-61400-1
3-527-61401-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chiral Auxiliaries in Cycloadditions; Table of Contents; 1 [2+1] Cycloadditions (Cyclopropanations); 1.1 Simmons-Smith Reactions; 1.2 Cyclopropanations with Carbene Equivalents; 1.3 Cyclopropanations with Ylide Reagents; 1.3.1 Chiral Ylide Reagents; 1.3.2 Chiral Alkenes; 1.4 Transition Metal-Catalyzed Reactions of Diazo Compounds; 1.5 References; 2 [2+2] Cycloadditions; 2.1 Reactions of Imines with Ketenes (Staudinger Reaction); 2.1.1 Chiral Ketenes; 2.1.2 Chiral Imines; 2.2 Reactions of Keteniminium Salts with Alkenes; 2.3 Reactions of Ketenes with Electronrich Alkenes; 2.3.1 Chiral Ketenes
2.3.2 Chiral Vinylethers2.3.3 Miscellaneous Reactions; 2.4 Reactions of Isocyanates with Alkenes; 2.5 Photochemically Induced [2+2] Cycloadditions; 2.5.1 Paterno-Büchi Reactions; 2.5.2 Application of Chromium Carbene Complexes; 2.6 References; 3 [4+2] Cycloadditions (Diels-Alder Reactions); 3.1 Thermal Reactions; 3.1.1 Reactions of Chiral Dienophiles; 3.1.2 Reactions of Achiral Dienophiles with Chiral Dienes; 3.2 Lewis Acid-Catalyzed Reactions; 3.2.1 Reactions of Chiral Dienophiles; 3.2.2 Reactions of Achiral Dienophiles with Chiral Dienes; 3.3 Intramolecular [4+2] Cycloadditions
3.3.1 Thermal Reactions3.3.2 Lewis Acid-Catalyzed Reactions; 3.4 References; 4 Hetero [4+2] Cycloadditions; 4.1 Reactions of Hetero-Dienophiles with Dienes; 4.1.1 Reactions of Activated Carbonyl Dienophiles/Aldehydes; 4.1.1 . 1 Reactions of Chiral Carbonyl Dienophiles with Achiral Dienes; 4.1.1.2 Reactions of Achiral Carbonyl Dienophiles with Chiral Heteroatom-substituted Dienes; 4.1.2 Reactions of Imines; 4.1.2.1 Reactions of Chiral Imines with Dienes; 4.1.2.2 Reactions of Chiral Imines with Heteroatom-substituted Dienes
4.1.2.3 Reactions of Achiral Imines with Chiral Heteroatom-substituted Dienes4.1.3 Reactions of Nitroso Compounds; 4.1.3.1 Reactions of Chloronitroso Compounds; 4.1.4 Reactions of N-Acylnitroso Compounds; 4.1.4.1 Reactions of Chiral N-Acylnitroso Compounds with Dienes; 4.1.4.2 Reactions of Achiral N-Acylnitroso Compounds with Achiral Dienes; 4.1.5 Reactions of N-Sulfinyl Dienophiles; 4.1.6 Reactions of N=N Dienophiles; 4.2 Reactions of Hetero-Dienes with Dienophiles; 4.2.1 Reactions of Oxabutadienes; 4.2.1.1 Reactions of Chiral Oxabutadienes with Achiral Vinylethers
4.2.1.2 Reactions of Achiral Oxabutadienes with Chiral Vinylethers4.2.2 Reactions of Achiral Nitroso Compounds; 4.2.3 Reactions of Nitroalkenes; 4.2.4 Reactions of 1-Aza-1,3-dienes; 4.2.5 Reactions of 2-Aza-1,3-dienes; 4.2.6 Reactions of Chiral N-Acyl-Imines; 4.2.7 Reactions of Thiabutadienes; 4.2.8 Intramolecular Hetero [4+2] Cycloadditions; 4.3 References; 5 [3+2] Cycloadditions; 5.1 Chiral Dipolarophiles; 5.1.1 Reactions of Nitrile Oxides; 5.1.2 Reactions of Nitrile Imines; 5.1.3 Reactions of Nitrones; 5.1.4 Reactions of Nitronates; 5.1.5 Reactions of Azomethine Ylides
5.1.5.1 Reactions of Azomethine Ylides Derived from AIdimines
Record Nr. UNINA-9910144281703321
Rück-Braun Karola  
Weinheim, [Germany] : , : Wiley-VCH, , 1999
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral auxiliaries in cycloadditions / / Karola Ruck-Braun, Horst Kunz
Chiral auxiliaries in cycloadditions / / Karola Ruck-Braun, Horst Kunz
Autore Rück-Braun Karola
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH, , 1999
Descrizione fisica 1 online resource (190 p.)
Disciplina 547.2
547.504593
Soggetto topico Chirality
Ring formation (Chemistry)
Organic compounds - Synthesis
ISBN 1-281-84251-6
9786611842512
3-527-61400-1
3-527-61401-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chiral Auxiliaries in Cycloadditions; Table of Contents; 1 [2+1] Cycloadditions (Cyclopropanations); 1.1 Simmons-Smith Reactions; 1.2 Cyclopropanations with Carbene Equivalents; 1.3 Cyclopropanations with Ylide Reagents; 1.3.1 Chiral Ylide Reagents; 1.3.2 Chiral Alkenes; 1.4 Transition Metal-Catalyzed Reactions of Diazo Compounds; 1.5 References; 2 [2+2] Cycloadditions; 2.1 Reactions of Imines with Ketenes (Staudinger Reaction); 2.1.1 Chiral Ketenes; 2.1.2 Chiral Imines; 2.2 Reactions of Keteniminium Salts with Alkenes; 2.3 Reactions of Ketenes with Electronrich Alkenes; 2.3.1 Chiral Ketenes
2.3.2 Chiral Vinylethers2.3.3 Miscellaneous Reactions; 2.4 Reactions of Isocyanates with Alkenes; 2.5 Photochemically Induced [2+2] Cycloadditions; 2.5.1 Paterno-Büchi Reactions; 2.5.2 Application of Chromium Carbene Complexes; 2.6 References; 3 [4+2] Cycloadditions (Diels-Alder Reactions); 3.1 Thermal Reactions; 3.1.1 Reactions of Chiral Dienophiles; 3.1.2 Reactions of Achiral Dienophiles with Chiral Dienes; 3.2 Lewis Acid-Catalyzed Reactions; 3.2.1 Reactions of Chiral Dienophiles; 3.2.2 Reactions of Achiral Dienophiles with Chiral Dienes; 3.3 Intramolecular [4+2] Cycloadditions
3.3.1 Thermal Reactions3.3.2 Lewis Acid-Catalyzed Reactions; 3.4 References; 4 Hetero [4+2] Cycloadditions; 4.1 Reactions of Hetero-Dienophiles with Dienes; 4.1.1 Reactions of Activated Carbonyl Dienophiles/Aldehydes; 4.1.1 . 1 Reactions of Chiral Carbonyl Dienophiles with Achiral Dienes; 4.1.1.2 Reactions of Achiral Carbonyl Dienophiles with Chiral Heteroatom-substituted Dienes; 4.1.2 Reactions of Imines; 4.1.2.1 Reactions of Chiral Imines with Dienes; 4.1.2.2 Reactions of Chiral Imines with Heteroatom-substituted Dienes
4.1.2.3 Reactions of Achiral Imines with Chiral Heteroatom-substituted Dienes4.1.3 Reactions of Nitroso Compounds; 4.1.3.1 Reactions of Chloronitroso Compounds; 4.1.4 Reactions of N-Acylnitroso Compounds; 4.1.4.1 Reactions of Chiral N-Acylnitroso Compounds with Dienes; 4.1.4.2 Reactions of Achiral N-Acylnitroso Compounds with Achiral Dienes; 4.1.5 Reactions of N-Sulfinyl Dienophiles; 4.1.6 Reactions of N=N Dienophiles; 4.2 Reactions of Hetero-Dienes with Dienophiles; 4.2.1 Reactions of Oxabutadienes; 4.2.1.1 Reactions of Chiral Oxabutadienes with Achiral Vinylethers
4.2.1.2 Reactions of Achiral Oxabutadienes with Chiral Vinylethers4.2.2 Reactions of Achiral Nitroso Compounds; 4.2.3 Reactions of Nitroalkenes; 4.2.4 Reactions of 1-Aza-1,3-dienes; 4.2.5 Reactions of 2-Aza-1,3-dienes; 4.2.6 Reactions of Chiral N-Acyl-Imines; 4.2.7 Reactions of Thiabutadienes; 4.2.8 Intramolecular Hetero [4+2] Cycloadditions; 4.3 References; 5 [3+2] Cycloadditions; 5.1 Chiral Dipolarophiles; 5.1.1 Reactions of Nitrile Oxides; 5.1.2 Reactions of Nitrile Imines; 5.1.3 Reactions of Nitrones; 5.1.4 Reactions of Nitronates; 5.1.5 Reactions of Azomethine Ylides
5.1.5.1 Reactions of Azomethine Ylides Derived from AIdimines
Record Nr. UNINA-9910830972803321
Rück-Braun Karola  
Weinheim, [Germany] : , : Wiley-VCH, , 1999
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cycloaddition Reactions in Organic Synthesis
Cycloaddition Reactions in Organic Synthesis
Autore Kobayashi Shu
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH Imprint, 2002
Descrizione fisica 1 online resource (337 pages)
Disciplina 547.2
Soggetto topico Ring formation (Chemistry)
Organic compounds - Synthesis
ISBN 1-280-55769-9
9786610557691
3-527-60025-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction Catalytic Asymmetric Diels--Alder Reactions Recent Advances in Palladium--catalyzed Cycloadditions Involving Trimethylenemethane and its Analogs Enantioselective [2+1] Cycloaddition: Cyclopropanation with Zinc Carbenoids Catalytic Enantioselective Cycloaddition Reactions of Carbonyl Compounds Catalytic Enantioselective Aza Diels--Alder Reactions Asymmetric Metal--catalyzed 1,3--Dipolar Cycloaddition Reactions Aqua Complex Lewis Acid Catalysts for Asymmetric 3+2 Cycloaddition Reactions Theoretical Calculations of Metal--catalyzed Cycloaddition Reactions Index.
Record Nr. UNINA-9910830589203321
Kobayashi Shu  
[Place of publication not identified], : Wiley VCH Imprint, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cycloaddition Reactions in Organic Synthesis
Cycloaddition Reactions in Organic Synthesis
Autore Kobayashi Shu
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH Imprint, 2002
Descrizione fisica 1 online resource (337 pages)
Disciplina 547.2
Soggetto topico Ring formation (Chemistry)
Organic compounds - Synthesis
ISBN 1-280-55769-9
9786610557691
3-527-60025-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction Catalytic Asymmetric Diels--Alder Reactions Recent Advances in Palladium--catalyzed Cycloadditions Involving Trimethylenemethane and its Analogs Enantioselective [2+1] Cycloaddition: Cyclopropanation with Zinc Carbenoids Catalytic Enantioselective Cycloaddition Reactions of Carbonyl Compounds Catalytic Enantioselective Aza Diels--Alder Reactions Asymmetric Metal--catalyzed 1,3--Dipolar Cycloaddition Reactions Aqua Complex Lewis Acid Catalysts for Asymmetric 3+2 Cycloaddition Reactions Theoretical Calculations of Metal--catalyzed Cycloaddition Reactions Index.
Record Nr. UNINA-9910840996003321
Kobayashi Shu  
[Place of publication not identified], : Wiley VCH Imprint, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Indole ring synthesis : from natural products to drug discovery / / Gordon W. Gribble
Indole ring synthesis : from natural products to drug discovery / / Gordon W. Gribble
Autore Gribble Gordon W.
Pubbl/distr/stampa Chichester, [England] : , : Wiley, , 2016
Descrizione fisica 1 online resource (707 p.)
Disciplina 661/.816
Soggetto topico Organic compounds - Synthesis
Indole
Ring formation (Chemistry)
Transition metal catalysts
Soggetto genere / forma Electronic books.
ISBN 1-118-68385-4
1-118-69569-0
1-118-68305-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 26 Cadogan-Sundberg Indole SynthesisChapter 27 Sundberg Indole Synthesis; Chapter 28 Hemetsberger Indole Synthesis; Chapter 29 Taber Indole Synthesis; Chapter 30 Knochel Indole Synthesis; Chapter 31 Täuber Carbazole Synthesis; Chapter 32 Quéguiner Azacarbazole Synthesis; Chapter 33 Iwao Indole Synthesis; Chapter 34 Hewson Indole Synthesis; Chapter 35 Magnus Indole Synthesis; Chapter 36 Feldman Indole Synthesis; Chapter 37 Butin Indole Synthesis; Chapter 38 Miscellaneous Electrophilic Cyclizations; Chapter 39 Nenitzescu o,β-Dinitrostyrene Reductive Cyclization
Chapter 52 Miscellaneous Radical-Promoted Indole Syntheses
Record Nr. UNINA-9910134877703321
Gribble Gordon W.  
Chichester, [England] : , : Wiley, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Indole ring synthesis : from natural products to drug discovery / / Gordon W. Gribble
Indole ring synthesis : from natural products to drug discovery / / Gordon W. Gribble
Autore Gribble Gordon W.
Pubbl/distr/stampa Chichester, [England] : , : Wiley, , 2016
Descrizione fisica 1 online resource (707 p.)
Disciplina 661/.816
Soggetto topico Organic compounds - Synthesis
Indole
Ring formation (Chemistry)
Transition metal catalysts
ISBN 1-118-68385-4
1-118-69569-0
1-118-68305-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 52 Miscellaneous Radical-Promoted Indole Syntheses
Record Nr. UNINA-9910830781103321
Gribble Gordon W.  
Chichester, [England] : , : Wiley, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2014
Descrizione fisica 1 online resource (673 p.)
Disciplina 547/.27
Altri autori (Persone) NishiwakiNagatoshi <1963->
Soggetto topico Organic compounds - Synthesis
Ring formation (Chemistry)
ISBN 1-118-77820-0
1-118-77817-0
1-118-77818-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Methods and Applications of Cycloaddition Reactions in Organic Syntheses; Contents; Preface; Contributors; Part I: [2+1] Cycloaddition; 1 [2+1]-Type Cyclopropanation Reactions; 1.1 INTRODUCTION; 1.2 CYCLOPROPANATION REACTION VIA MICHAEL-INDUCED RING CLOSURE REACTION; 1.2.1 Introduction; 1.2.2 Halo-Substituted Nucleophiles in MIRC Reaction; 1.2.3 Ylides for Cyclopropanation; 1.3 SIMMONS-SMITH CYCLOPROPANATION AND RELATED REACTIONS; 1.3.1 Introduction; 1.3.2 The Simmons-Smith Reaction with Zinc Reagents; 1.4 DIAZOALKANES WITH TRANSITION METAL CATALYSTS; 1.4.1 Introduction
1.4.2 Rhodium-Catalyzed Reactions1.4.4 Ruthenium-Catalyzed Reactions; 1.4.5 Cobalt- and Iron-Catalyzed Reactions; 1.4.6 Other Transition Metal-Catalyzed Reactions; 1.4.7 Cyclopropanation Without Transition Metal Catalysts; 1.4.8 Cyclopropanation of Dihalocarbenes; 1.5 CYCLOISOMERIZATION WITH TRANSITION METAL CATALYSTS; 1.5.1 Introduction; 1.5.2 Gold Complex-Catalyzed Reactions; 1.5.3 Palladium Complex-Catalyzed Reactions; 1.5.4 Platinum Complex-Catalyzed Reactions; 1.5.5 Ruthenium Complex-Catalyzed Reactions; 1.5.6 Other Metal Complex-Catalyzed Reactions; 1.6 KULINKOVICH REACTIONS
1.6.1 Introduction1.6.2 The Kulinkovich Reaction to Esters, Ketones, and Amides; 1.6.3 Kulinkovich Reaction to Nitriles; 1.6.4 Other Ti-Mediated Cyclopropanation Reactions; 1.7 MISCELLANEOUS [2+1]-TYPE OF CYCLOPROPANATION REACTIONS; REFERENCES; 2 N1 Unit Transfer Reaction To C-C Double Bonds; 2.1 INTRODUCTION; 2.2 AZIRIDINATION WITH AZIDES; 2.3 AZIRIDINATION WITH IMINOIODINANES; 2.4 AZIRIDINATION WITH N-HALOAMINE SALTS; 2.5 AZIRIDINATION WITH OTHER N1 UNIT; 2.6 CONCLUSIONS; REFERENCES; Part II: [2+2] Cycloaddition; 3 Lewis Base Catalyzed Asymmetric Formal [2+2] Cycloadditions
3.1 INTRODUCTION3.2 β-LACTAMS: FORMAL [2+2] CYCLOADDITIONS INVOLVING IMINES; 3.3 β-LACTONES I: FORMAL [2+2] CYCLOADDITIONS INVOLVING ALDEHYDES/KETONES; 3.4 β-LACTONES II: FORMAL [2+2] CYCLOADDITION OF KETENES LEADING TO KETENE DIMERS; 3.4.1 Introduction or or; 3.4.2 Homodimerization; 3.4.3 Heterodimerization; 3.5 MISCELLANEOUS FORMAL [2+2] ASYMMETRIC CYCLOADDITION PROCESSES; 3.5.1 Other Heterocyclic Classes-Introduction; 3.5.2 Asymmetric Formal [2+2] Cycloadditions; 3.6 CONCLUSIONS; REFERENCES; Part III: [2+2] and [4+2]/[2+2] Cycloaddition; 4 Catalytic [2+2] Cycloaddition of Silyl Enol Ethers
4.1 INTRODUCTION4.2 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY LEWIS ACID CATALYST; 4.2.1 Introduction; 4.2.2 Intramolecular [2+2] Cycloaddition Reactions; 4.2.3 Intermolecular [2+2] Cycloaddition Reactions; 4.2.4 Asymmetric Catalytic [2+2] Cycloaddition Reaction with Silyl Enol Ethers; 4.3 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY BRØNSTED ACID; 4.3.1 Catalytic [2+2] Cycloaddition Reactions of Silyl Enol Ethers by Trifluoromethanesulfonimide; 4.3.2 Multigram Syntheses of Cyclobutanes and Cyclobutenes by [2+2] Cycloaddition Reactions
4.3.3 Analysis of the Mechanism for [2+2] Cycloaddition Reactions by Trifluoromethanesulfonimide
Record Nr. UNINA-9910138976903321
Hoboken, New Jersey : , : Wiley, , 2014
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Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
Methods and applications of cycloaddition reactions in organic syntheses / / edited by Nagatoshi Nishiwaki
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2014
Descrizione fisica 1 online resource (673 p.)
Disciplina 547/.27
Altri autori (Persone) NishiwakiNagatoshi <1963->
Soggetto topico Organic compounds - Synthesis
Ring formation (Chemistry)
ISBN 1-118-77820-0
1-118-77817-0
1-118-77818-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Methods and Applications of Cycloaddition Reactions in Organic Syntheses; Contents; Preface; Contributors; Part I: [2+1] Cycloaddition; 1 [2+1]-Type Cyclopropanation Reactions; 1.1 INTRODUCTION; 1.2 CYCLOPROPANATION REACTION VIA MICHAEL-INDUCED RING CLOSURE REACTION; 1.2.1 Introduction; 1.2.2 Halo-Substituted Nucleophiles in MIRC Reaction; 1.2.3 Ylides for Cyclopropanation; 1.3 SIMMONS-SMITH CYCLOPROPANATION AND RELATED REACTIONS; 1.3.1 Introduction; 1.3.2 The Simmons-Smith Reaction with Zinc Reagents; 1.4 DIAZOALKANES WITH TRANSITION METAL CATALYSTS; 1.4.1 Introduction
1.4.2 Rhodium-Catalyzed Reactions1.4.4 Ruthenium-Catalyzed Reactions; 1.4.5 Cobalt- and Iron-Catalyzed Reactions; 1.4.6 Other Transition Metal-Catalyzed Reactions; 1.4.7 Cyclopropanation Without Transition Metal Catalysts; 1.4.8 Cyclopropanation of Dihalocarbenes; 1.5 CYCLOISOMERIZATION WITH TRANSITION METAL CATALYSTS; 1.5.1 Introduction; 1.5.2 Gold Complex-Catalyzed Reactions; 1.5.3 Palladium Complex-Catalyzed Reactions; 1.5.4 Platinum Complex-Catalyzed Reactions; 1.5.5 Ruthenium Complex-Catalyzed Reactions; 1.5.6 Other Metal Complex-Catalyzed Reactions; 1.6 KULINKOVICH REACTIONS
1.6.1 Introduction1.6.2 The Kulinkovich Reaction to Esters, Ketones, and Amides; 1.6.3 Kulinkovich Reaction to Nitriles; 1.6.4 Other Ti-Mediated Cyclopropanation Reactions; 1.7 MISCELLANEOUS [2+1]-TYPE OF CYCLOPROPANATION REACTIONS; REFERENCES; 2 N1 Unit Transfer Reaction To C-C Double Bonds; 2.1 INTRODUCTION; 2.2 AZIRIDINATION WITH AZIDES; 2.3 AZIRIDINATION WITH IMINOIODINANES; 2.4 AZIRIDINATION WITH N-HALOAMINE SALTS; 2.5 AZIRIDINATION WITH OTHER N1 UNIT; 2.6 CONCLUSIONS; REFERENCES; Part II: [2+2] Cycloaddition; 3 Lewis Base Catalyzed Asymmetric Formal [2+2] Cycloadditions
3.1 INTRODUCTION3.2 β-LACTAMS: FORMAL [2+2] CYCLOADDITIONS INVOLVING IMINES; 3.3 β-LACTONES I: FORMAL [2+2] CYCLOADDITIONS INVOLVING ALDEHYDES/KETONES; 3.4 β-LACTONES II: FORMAL [2+2] CYCLOADDITION OF KETENES LEADING TO KETENE DIMERS; 3.4.1 Introduction or or; 3.4.2 Homodimerization; 3.4.3 Heterodimerization; 3.5 MISCELLANEOUS FORMAL [2+2] ASYMMETRIC CYCLOADDITION PROCESSES; 3.5.1 Other Heterocyclic Classes-Introduction; 3.5.2 Asymmetric Formal [2+2] Cycloadditions; 3.6 CONCLUSIONS; REFERENCES; Part III: [2+2] and [4+2]/[2+2] Cycloaddition; 4 Catalytic [2+2] Cycloaddition of Silyl Enol Ethers
4.1 INTRODUCTION4.2 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY LEWIS ACID CATALYST; 4.2.1 Introduction; 4.2.2 Intramolecular [2+2] Cycloaddition Reactions; 4.2.3 Intermolecular [2+2] Cycloaddition Reactions; 4.2.4 Asymmetric Catalytic [2+2] Cycloaddition Reaction with Silyl Enol Ethers; 4.3 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY BRØNSTED ACID; 4.3.1 Catalytic [2+2] Cycloaddition Reactions of Silyl Enol Ethers by Trifluoromethanesulfonimide; 4.3.2 Multigram Syntheses of Cyclobutanes and Cyclobutenes by [2+2] Cycloaddition Reactions
4.3.3 Analysis of the Mechanism for [2+2] Cycloaddition Reactions by Trifluoromethanesulfonimide
Record Nr. UNINA-9910828347603321
Hoboken, New Jersey : , : Wiley, , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui