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Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey
| Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
| Descrizione fisica | 1 online resource (774 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Wiley series on comprehensive name reactions |
| Soggetto topico | Ring formation (Chemistry) |
| ISBN |
1-299-31411-2
0-470-87221-7 0-470-87220-9 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Carbocyclic Ring Formations; Contents; Foreword; Preface; Contributing Authors; Chapter 1 Three-Membered Carbocycles; 1.1 Freund Reaction; 1.2 Kishner Cyclopropane Synthesis; 1.3 Kulinovich Cyclopropanol Synthesis; 1.4 Simmons-Smith Cyclopropanation; Chapter 2 Four-Membered Carbocycles; 2.1 Staudinger Ketene Cycloaddition; Chapter 3 Five-Membered Carbocycles; 3.1 Danheiser Annulation; 3.2 Dieckmann Condensation; 3.3 Favorskii Rearrangement; 3.4 Nazarov Cyclization; 3.5 Pauson-Khand Reaction; 3.6 Weiss-Cook Reaction; Chapter 4 Six-Membered Carbocycles
4.1 Bardhan-Sengupta Pheantherene Synthesis4.2 Bergman Cyclization; 4.3 Bogert-Cook Reaction; 4.4 Bradsher Cycloaddition and Bradsher Reaction; 4.5 Bradsher Reaction; 4.6 Darzens Synthesis of Tetralin Derivatives; 4.7 Diels-Alder Reaction; 4.8 Dötz Benzannulation; 4.9 Elbs Reaction; 4.10 Fujimoto-Belleau Reaction; 4.11 Haworth Reaction; 4.12 Moore Cyclization; 4.13 Myers-Saito Cyclization; 4.14 Robinson Annulation; 4.15 Scholl Reaction; Chapter 5 Large-Ring Carbocycles; 5.1 Buchner Reaction; 5.2 de Mayo Reaction; 5.3 Ring-closing Metathesis (RCM); 5.4 Thorpe-Ziegler Reaction Chapter 6 Transformations of Carbocycles 6.1 Blanc Chloromethylation Reaction; 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present; 6.3 Houben-Hoesch Reaction; 6.4 Kolbe-Schmitt Reaction; 6.5 Vilsmeier-Haack Reaction; 6.6 von Richter Reaction; Appendices; 1, Contents Volume 1: Name Reactions in Heterocyclic Chemistry; 2, Contents Volume 2: Name Reactions for Functional Group Transformations; 3, Contents Volume 3: Name Reactions for Homologations-Part I; 4, Contents Volume 4: Name Reactions for Homologations-Part II; 5, Contents Volume 6: Name Reactions in Heterocyclic Chemistry-Part II Subject Index |
| Record Nr. | UNINA-9910140873403321 |
| Hoboken, N.J., : Wiley, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey
| Name reactions for carbocyclic ring formations [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
| Descrizione fisica | 1 online resource (774 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Wiley series on comprehensive name reactions |
| Soggetto topico | Ring formation (Chemistry) |
| ISBN |
1-299-31411-2
0-470-87221-7 0-470-87220-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Carbocyclic Ring Formations; Contents; Foreword; Preface; Contributing Authors; Chapter 1 Three-Membered Carbocycles; 1.1 Freund Reaction; 1.2 Kishner Cyclopropane Synthesis; 1.3 Kulinovich Cyclopropanol Synthesis; 1.4 Simmons-Smith Cyclopropanation; Chapter 2 Four-Membered Carbocycles; 2.1 Staudinger Ketene Cycloaddition; Chapter 3 Five-Membered Carbocycles; 3.1 Danheiser Annulation; 3.2 Dieckmann Condensation; 3.3 Favorskii Rearrangement; 3.4 Nazarov Cyclization; 3.5 Pauson-Khand Reaction; 3.6 Weiss-Cook Reaction; Chapter 4 Six-Membered Carbocycles
4.1 Bardhan-Sengupta Pheantherene Synthesis4.2 Bergman Cyclization; 4.3 Bogert-Cook Reaction; 4.4 Bradsher Cycloaddition and Bradsher Reaction; 4.5 Bradsher Reaction; 4.6 Darzens Synthesis of Tetralin Derivatives; 4.7 Diels-Alder Reaction; 4.8 Dötz Benzannulation; 4.9 Elbs Reaction; 4.10 Fujimoto-Belleau Reaction; 4.11 Haworth Reaction; 4.12 Moore Cyclization; 4.13 Myers-Saito Cyclization; 4.14 Robinson Annulation; 4.15 Scholl Reaction; Chapter 5 Large-Ring Carbocycles; 5.1 Buchner Reaction; 5.2 de Mayo Reaction; 5.3 Ring-closing Metathesis (RCM); 5.4 Thorpe-Ziegler Reaction Chapter 6 Transformations of Carbocycles 6.1 Blanc Chloromethylation Reaction; 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present; 6.3 Houben-Hoesch Reaction; 6.4 Kolbe-Schmitt Reaction; 6.5 Vilsmeier-Haack Reaction; 6.6 von Richter Reaction; Appendices; 1, Contents Volume 1: Name Reactions in Heterocyclic Chemistry; 2, Contents Volume 2: Name Reactions for Functional Group Transformations; 3, Contents Volume 3: Name Reactions for Homologations-Part I; 4, Contents Volume 4: Name Reactions for Homologations-Part II; 5, Contents Volume 6: Name Reactions in Heterocyclic Chemistry-Part II Subject Index |
| Record Nr. | UNINA-9910820978603321 |
| Hoboken, N.J., : Wiley, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey
| Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2007 |
| Descrizione fisica | 1 online resource (769 p.) |
| Disciplina |
547
547/.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Comprehensive Name Reactions |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-93539-1
9786610935390 0-470-17651-2 0-470-17650-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric synthesis. CBS reduction ; Davis chiral oxaziridine reagents ; Midland reduction ; Noyori catalytic asymmetric hydrogenation ; Sharpless asymmetric hydroxylation reactions -- Reduction. Eschweiler-Clark reductive alkylation of amines ; Gribble reduction of diaryl ketones ; Luche reduction ; Meerwein-Ponndorf-Verley reduction ; Staudinger reaction ; Wharton reaction -- Oxidation. Baeyer-Villiger oxidation ; Brown hydroboration reaction ; Burgess dehydrating reagent ; Corey-Kim oxidation ; Dess-Martin periodinane oxidation ; Tamao-Kumada-Fleming oxidation ; Martin's sulfurane dehydrating reagent ; Oppenauer oxidation ; Prilezhaev reaction ; Rubottom oxidation ; Swern oxidation ; Wacker-Tsuji oxidation ; Woodward cis-dihydroxylation --
Olefination. Chugaev elimination ; Cope elimination reaction ; Corey-Winter olefin synthesis ; Perkin reaction (cinnamic acid synthesis) ; Perkow vinyl phosphate synthesis ; Ramberg-Bäcklund olefin synthesis ; Shapiro reaction ; Zaitsev elimination -- Amine synthesis. Fukuyama amine synthesis ; Gabriel synthesis ; Leuckart-Wallach reaction -- Carboxylic acid derivatives synthesis. Fischer-Speier esterification ; Mukaiyama esterification ; Ritter reaction ; Strecker amino acid synthesis ; Yamada coupling reagent ; Yamaguchi esterification -- Miscellaneous functional group manipulations. Balz-Schiemann reaction ; Buchwald-Hartwig reactions ; Haloform reaction ; Hunsdiecker reaction ; Japp-Klingemann hydrazone synthesis ; Krapcho decarboxylation ; Nef reaction ; Prins reaction ; Regitz diazo synthesis ; Sommelet reaction. |
| Record Nr. | UNINA-9910143425703321 |
| Hoboken, N.J., : Wiley-Interscience, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey
| Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2007 |
| Descrizione fisica | 1 online resource (769 p.) |
| Disciplina |
547
547/.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Comprehensive Name Reactions |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| ISBN |
1-280-93539-1
9786610935390 0-470-17651-2 0-470-17650-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric synthesis. CBS reduction ; Davis chiral oxaziridine reagents ; Midland reduction ; Noyori catalytic asymmetric hydrogenation ; Sharpless asymmetric hydroxylation reactions -- Reduction. Eschweiler-Clark reductive alkylation of amines ; Gribble reduction of diaryl ketones ; Luche reduction ; Meerwein-Ponndorf-Verley reduction ; Staudinger reaction ; Wharton reaction -- Oxidation. Baeyer-Villiger oxidation ; Brown hydroboration reaction ; Burgess dehydrating reagent ; Corey-Kim oxidation ; Dess-Martin periodinane oxidation ; Tamao-Kumada-Fleming oxidation ; Martin's sulfurane dehydrating reagent ; Oppenauer oxidation ; Prilezhaev reaction ; Rubottom oxidation ; Swern oxidation ; Wacker-Tsuji oxidation ; Woodward cis-dihydroxylation --
Olefination. Chugaev elimination ; Cope elimination reaction ; Corey-Winter olefin synthesis ; Perkin reaction (cinnamic acid synthesis) ; Perkow vinyl phosphate synthesis ; Ramberg-Bäcklund olefin synthesis ; Shapiro reaction ; Zaitsev elimination -- Amine synthesis. Fukuyama amine synthesis ; Gabriel synthesis ; Leuckart-Wallach reaction -- Carboxylic acid derivatives synthesis. Fischer-Speier esterification ; Mukaiyama esterification ; Ritter reaction ; Strecker amino acid synthesis ; Yamada coupling reagent ; Yamaguchi esterification -- Miscellaneous functional group manipulations. Balz-Schiemann reaction ; Buchwald-Hartwig reactions ; Haloform reaction ; Hunsdiecker reaction ; Japp-Klingemann hydrazone synthesis ; Krapcho decarboxylation ; Nef reaction ; Prins reaction ; Regitz diazo synthesis ; Sommelet reaction. |
| Record Nr. | UNINA-9910830062003321 |
| Hoboken, N.J., : Wiley-Interscience, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey
| Name reactions for functional group transformations [[electronic resource] /] / edited by Jie Jack Li, E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2007 |
| Descrizione fisica | 1 online resource (769 p.) |
| Disciplina |
547
547/.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Comprehensive Name Reactions |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions |
| ISBN |
1-280-93539-1
9786610935390 0-470-17651-2 0-470-17650-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Asymmetric synthesis. CBS reduction ; Davis chiral oxaziridine reagents ; Midland reduction ; Noyori catalytic asymmetric hydrogenation ; Sharpless asymmetric hydroxylation reactions -- Reduction. Eschweiler-Clark reductive alkylation of amines ; Gribble reduction of diaryl ketones ; Luche reduction ; Meerwein-Ponndorf-Verley reduction ; Staudinger reaction ; Wharton reaction -- Oxidation. Baeyer-Villiger oxidation ; Brown hydroboration reaction ; Burgess dehydrating reagent ; Corey-Kim oxidation ; Dess-Martin periodinane oxidation ; Tamao-Kumada-Fleming oxidation ; Martin's sulfurane dehydrating reagent ; Oppenauer oxidation ; Prilezhaev reaction ; Rubottom oxidation ; Swern oxidation ; Wacker-Tsuji oxidation ; Woodward cis-dihydroxylation --
Olefination. Chugaev elimination ; Cope elimination reaction ; Corey-Winter olefin synthesis ; Perkin reaction (cinnamic acid synthesis) ; Perkow vinyl phosphate synthesis ; Ramberg-Bäcklund olefin synthesis ; Shapiro reaction ; Zaitsev elimination -- Amine synthesis. Fukuyama amine synthesis ; Gabriel synthesis ; Leuckart-Wallach reaction -- Carboxylic acid derivatives synthesis. Fischer-Speier esterification ; Mukaiyama esterification ; Ritter reaction ; Strecker amino acid synthesis ; Yamada coupling reagent ; Yamaguchi esterification -- Miscellaneous functional group manipulations. Balz-Schiemann reaction ; Buchwald-Hartwig reactions ; Haloform reaction ; Hunsdiecker reaction ; Japp-Klingemann hydrazone synthesis ; Krapcho decarboxylation ; Nef reaction ; Prins reaction ; Regitz diazo synthesis ; Sommelet reaction. |
| Record Nr. | UNINA-9910840575103321 |
| Hoboken, N.J., : Wiley-Interscience, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions in heterocyclic chemistry II [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey
| Name reactions in heterocyclic chemistry II [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2011 |
| Descrizione fisica | 1 online resource (706 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Wiley series on comprehensive name reactions |
| Soggetto topico |
Heterocyclic chemistry
Chemical reactions |
| ISBN |
1-283-28270-4
9786613282705 1-118-09284-8 1-118-09285-6 1-118-09282-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions in Heterocyclic Chemistry II; Contents; Foreword; Preface; Contributing Authors; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Aziridines and Epoxides; 1.1 Blum Aziridine Synthesis; 1.2 Gabriel-Heine Aziridine Isomerization; 1.3 Shi Epoxidation; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Clauson-Kass Pyrrole Synthesis; 2.2 Houben-Hoesch Acylation of Pyrroles; 2.3 Overman Pyrrolidine Synthesis; 2.4 Trofimov Synthesis of Pyrroles; Chapter 3 Indoles; 3.1 Bischler-Möhlau Indole Synthesis; 3.2 Borsche-Drechsel Cyclization
3.3 Buchwald-Hartwig Indole Synthesis 3.4 Cadogan-Sundberg Indole Synthesis; 3.5 Fukuyama Indole Synthesis; 3.6 Gassman Oxindole Synthesis; 3.7 Larock Indole Synthesis; 3.8 Matinet Dioxindole Reaction; 3.9 Mori-Ban Indole Synthesis; 3.10 Sandmeyer Isatin Synthesis; 3.11 Sommelet-Hauser Rearrangement; 3.12 Stollé Oxindole Synthesis; Chapter 4 Furans and Oxazoles; 4.1 Nierenstein Reaction; 4.2 Davidson Oxazole Synthesis; 4.3 Fischer Oxazole Synthesis; 4.4 Japp Oxazole Synthesis; 4.5 Schöllkopf Oxazole Synthesis; Chapter 5 Other Five-Membered Heterocycles; 5.1 Bamberger Imidazole Cleavage 5.2 Dimroth Triazole Synthesis 5.3 Finnegan Tetrazole Synthesis; 5.4 Hantzsch Thiazole Synthesis; 5.5 Huisgen Tetrazole Rearrangement; 5.6 Knorr Pyrazole Synthesis; 5.7 Pechmann Pyrazole Synthesis; PART 3 SIX-MEMBERED HETEROCYCLES; Chapter 6 Pyridines; 6.1 Baeyer Pyridine Synthesis; 6.2 Katrizky Pyridine Synthesis; Chapter 7 Quinolines and Isoquinolines; 7.1 Betti Reaction; 7.2 Bernthsen Acridine Synthesis; 7.3 Lehmstedt- Tănăsescu Reaction; 7.4 Niementowski Quinoline Synthesis; 7.5 Povarov Reaction; Chapter 8 Six-Membered Heterocycles; 8.1 Balaban-Nenitzescu-Praill Reaction 8.2 Borsche Cinnoline Synthesis 8.3 Gutknecht Pyrazine Synthesis; 8.4 Niementowski Quinazoline Synthesis; 8.5 Pechmann Coumarin Synthesis; 8.6 Robinson-Schöpf Condensation; 8.7 Simonis Chromone Cyclization; 8.8 Wesseley-Moser Rearrangement; 8.9 Widman-Stoermer Cinnoline Synthesis; 8.10 Wichterle Reaction; Chapter 9 Miscellaneous Name Reactions; 9.1 ANRORC Mechanism; 9.2 Boulton-Katritzky Rearrangement; 9.3 Chichibabin Amination Reaction; 9.4 Dimroth Rearrangement; 9.5 Hantzsch Synthesis; 9.6 Ortoleva-King Reaction; Appendixes Appendix 1, Table of Contents for Volume 1 : Name Reactions in Heterocyclic Chemistry Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations; Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations-I; Appendix 4, Table of Contents for Volume 4: Name Reactions for Homologations-II; Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations; Subject Index |
| Record Nr. | UNINA-9910137998503321 |
| Hoboken, N.J., : Wiley, c2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions in heterocyclic chemistry II [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey
| Name reactions in heterocyclic chemistry II [[electronic resource] /] / edited by Jie Jack Li ; foreword by E.J. Corey |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2011 |
| Descrizione fisica | 1 online resource (706 p.) |
| Disciplina | 547.2 |
| Altri autori (Persone) |
LiJie Jack
CoreyE. J |
| Collana | Wiley series on comprehensive name reactions |
| Soggetto topico |
Heterocyclic chemistry
Chemical reactions |
| ISBN |
1-283-28270-4
9786613282705 1-118-09284-8 1-118-09285-6 1-118-09282-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions in Heterocyclic Chemistry II; Contents; Foreword; Preface; Contributing Authors; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Aziridines and Epoxides; 1.1 Blum Aziridine Synthesis; 1.2 Gabriel-Heine Aziridine Isomerization; 1.3 Shi Epoxidation; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Clauson-Kass Pyrrole Synthesis; 2.2 Houben-Hoesch Acylation of Pyrroles; 2.3 Overman Pyrrolidine Synthesis; 2.4 Trofimov Synthesis of Pyrroles; Chapter 3 Indoles; 3.1 Bischler-Möhlau Indole Synthesis; 3.2 Borsche-Drechsel Cyclization
3.3 Buchwald-Hartwig Indole Synthesis 3.4 Cadogan-Sundberg Indole Synthesis; 3.5 Fukuyama Indole Synthesis; 3.6 Gassman Oxindole Synthesis; 3.7 Larock Indole Synthesis; 3.8 Matinet Dioxindole Reaction; 3.9 Mori-Ban Indole Synthesis; 3.10 Sandmeyer Isatin Synthesis; 3.11 Sommelet-Hauser Rearrangement; 3.12 Stollé Oxindole Synthesis; Chapter 4 Furans and Oxazoles; 4.1 Nierenstein Reaction; 4.2 Davidson Oxazole Synthesis; 4.3 Fischer Oxazole Synthesis; 4.4 Japp Oxazole Synthesis; 4.5 Schöllkopf Oxazole Synthesis; Chapter 5 Other Five-Membered Heterocycles; 5.1 Bamberger Imidazole Cleavage 5.2 Dimroth Triazole Synthesis 5.3 Finnegan Tetrazole Synthesis; 5.4 Hantzsch Thiazole Synthesis; 5.5 Huisgen Tetrazole Rearrangement; 5.6 Knorr Pyrazole Synthesis; 5.7 Pechmann Pyrazole Synthesis; PART 3 SIX-MEMBERED HETEROCYCLES; Chapter 6 Pyridines; 6.1 Baeyer Pyridine Synthesis; 6.2 Katrizky Pyridine Synthesis; Chapter 7 Quinolines and Isoquinolines; 7.1 Betti Reaction; 7.2 Bernthsen Acridine Synthesis; 7.3 Lehmstedt- Tănăsescu Reaction; 7.4 Niementowski Quinoline Synthesis; 7.5 Povarov Reaction; Chapter 8 Six-Membered Heterocycles; 8.1 Balaban-Nenitzescu-Praill Reaction 8.2 Borsche Cinnoline Synthesis 8.3 Gutknecht Pyrazine Synthesis; 8.4 Niementowski Quinazoline Synthesis; 8.5 Pechmann Coumarin Synthesis; 8.6 Robinson-Schöpf Condensation; 8.7 Simonis Chromone Cyclization; 8.8 Wesseley-Moser Rearrangement; 8.9 Widman-Stoermer Cinnoline Synthesis; 8.10 Wichterle Reaction; Chapter 9 Miscellaneous Name Reactions; 9.1 ANRORC Mechanism; 9.2 Boulton-Katritzky Rearrangement; 9.3 Chichibabin Amination Reaction; 9.4 Dimroth Rearrangement; 9.5 Hantzsch Synthesis; 9.6 Ortoleva-King Reaction; Appendixes Appendix 1, Table of Contents for Volume 1 : Name Reactions in Heterocyclic Chemistry Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations; Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations-I; Appendix 4, Table of Contents for Volume 4: Name Reactions for Homologations-II; Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations; Subject Index |
| Record Nr. | UNINA-9910817213403321 |
| Hoboken, N.J., : Wiley, c2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Paeoniflorigenin and paeoniflorin.p. 633-640
| Paeoniflorigenin and paeoniflorin.p. 633-640 |
| Altri autori (Persone) | Corey, E.J. |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | und |
| Record Nr. | UNINA-990002353770403321 |
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
|
Prostaglandin F²ª (PGF²ª) and prostaglandin E² (PGE²).p. 65-82
| Prostaglandin F²ª (PGF²ª) and prostaglandin E² (PGE²).p. 65-82 |
| Altri autori (Persone) | Corey, E.J. |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | und |
| Record Nr. | UNINA-990002353500403321 |
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
|
The logic of chemical synthesis / E. J. Corey and Xue-Min Cheng
| The logic of chemical synthesis / E. J. Corey and Xue-Min Cheng |
| Autore | COREY, E. J. |
| Pubbl/distr/stampa | New York [etc.] : John Wiley & Sons, copyr. 1995 |
| Descrizione fisica | 436 p. : ill. ; 26 cm |
| Disciplina | 547.2 |
| Soggetto topico | Composti organici - Sintesi |
| ISBN | 0-471-11594-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-990001132710203316 |
COREY, E. J.
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| New York [etc.] : John Wiley & Sons, copyr. 1995 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
