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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 for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (874 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-11462-X
9786612114625 0-470-48704-6 0-470-48703-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part II; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Rearrangements; Section 1.1 Concerted rearrangement; 1.1.1 Alder ene reaction; 1.1.2 Claisen and related rearrangements; 1.1.3 Cope and related rearrangements; 1.1.4 Curtius rearrangement; 1.1.5 Hofmann rearrangement; 1.1.6 Lossen rearrangement; 1.1.7 Overman rearrangement; 1.1.8 [ 1,2]-Wittig rearrangement; 1.1.9 [2,3]-Wittig rearrangement; 1.1.10 Wolff rearrangement; Section 1.2 Cationic rearrangement; 1.2.1 Beckmann rearrangement; 1.2.2 Demjanov rearrangement
1.2.3 Meyer-Schuster rearrangement1.2.4 Pinacol rearrangement; 1.2.5 Pummerer rearrangement; 1.2.6 Schmidt rearrangement; 1.2.7 Wagner-Meerwein rearrangement; Section 1.3 Anionic rearrangement; 1.3.1 Benzilic acid rearrangement; 1.3.2 Brook rearrangement; 1.3.3 Favorskii rearrangement; 1.3.4 Grob fragmentation; 1.3.5 Neber rearrangement; 1.3.6 Payne rearrangement; 1.3.7 Smiles rearrangement; 1.3.8 Stevens rearrangement; Chapter 2. Asymmetric C-C bond formation; 2.1 Evans aldol reaction; 2.2 Hajos-Wiechert reaction; 2.3 Keck stereoselective allylation; 2.4 Roush allylboronation Chapter 3. Miscellaneous homologation reactions3.1 Bamford-Stevens reaction; 3.2 Mannich reaction; 3.3 Mitsunobu reaction; 3.4 Parham cyclization; 3.5 Passerini reaction; 3.6 Ugi 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 5: Name Reactions for Ring Formations Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-IISubject index |
| Record Nr. | UNINA-9910146415303321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (733 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-13765-4
9786612137655 0-470-48702-X 0-470-48701-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part I; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Organometallics; Section 1.1 Palladium Chemistry; 1.1.1 Heck reaction; 1.1.2 Hiyama cross-coupling reaction; 1.1.3 Kumada cross-coupling reaction; 1.1.4 Negishi cross-coupling reaction; 1.1.5 Sonogashira reaction; 1.1.6 Stille coupling; 1.1.7 Suzuki coupling; 1.1.8 Tsuji-Trost reaction; Section 1.2 Organocopper Reagents; 1.2.1 Castro-Stephens coupling; 1.2.2 Glaser coupling; 1.2.3 Ullmann reaction; Section 1.3 Other Organometallic Reagents; 1.3.1 McMurry coupling
1.3.2 Nicholas reaction1.3.3 Nozaki-Hiyama-Kishi reaction; 1.3.4 Tebbe olefination; Chapter 2. Carbon-Chain Homologations; 2.1 Arndt-Eistert homologation; 2.2 Morita-Baylis-Hillman reaction; 2.3 Benzoin condensation; 2.4 Corey-Fuchs reaction; 2.5 Henry reaction; 2.6 Horner-Wadsworth-Emmons reaction; 2.7 Julia-Lythgoe olefination; 2.8 Knoevenagel condensation; 2.9 Mukaiyama aldol reaction; 2.10 Peterson olefination; 2.11 Sakurai allylation reaction; 2.12 Stetter reaction; 2.13 Wittig reaction; Chapter 3. Radical Chemistry; 3.1 Barton-McCombie deoxygenation; 3.2 Barton nitrite photolysis 3.3 Sandmeyer reaction3.4 Wohl-Ziegler 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 4: Name Reactions for Homologations-2; Appendix 4, Table of Contents for Volume 5: Name Reactions for Ring Formations; Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-II; Subject index |
| Record Nr. | UNINA-9910146415603321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (733 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| ISBN |
1-282-13765-4
9786612137655 0-470-48702-X 0-470-48701-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part I; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Organometallics; Section 1.1 Palladium Chemistry; 1.1.1 Heck reaction; 1.1.2 Hiyama cross-coupling reaction; 1.1.3 Kumada cross-coupling reaction; 1.1.4 Negishi cross-coupling reaction; 1.1.5 Sonogashira reaction; 1.1.6 Stille coupling; 1.1.7 Suzuki coupling; 1.1.8 Tsuji-Trost reaction; Section 1.2 Organocopper Reagents; 1.2.1 Castro-Stephens coupling; 1.2.2 Glaser coupling; 1.2.3 Ullmann reaction; Section 1.3 Other Organometallic Reagents; 1.3.1 McMurry coupling
1.3.2 Nicholas reaction1.3.3 Nozaki-Hiyama-Kishi reaction; 1.3.4 Tebbe olefination; Chapter 2. Carbon-Chain Homologations; 2.1 Arndt-Eistert homologation; 2.2 Morita-Baylis-Hillman reaction; 2.3 Benzoin condensation; 2.4 Corey-Fuchs reaction; 2.5 Henry reaction; 2.6 Horner-Wadsworth-Emmons reaction; 2.7 Julia-Lythgoe olefination; 2.8 Knoevenagel condensation; 2.9 Mukaiyama aldol reaction; 2.10 Peterson olefination; 2.11 Sakurai allylation reaction; 2.12 Stetter reaction; 2.13 Wittig reaction; Chapter 3. Radical Chemistry; 3.1 Barton-McCombie deoxygenation; 3.2 Barton nitrite photolysis 3.3 Sandmeyer reaction3.4 Wohl-Ziegler 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 4: Name Reactions for Homologations-2; Appendix 4, Table of Contents for Volume 5: Name Reactions for Ring Formations; Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-II; Subject index |
| Record Nr. | UNINA-9910830063003321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (874 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| ISBN |
1-282-11462-X
9786612114625 0-470-48704-6 0-470-48703-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part II; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Rearrangements; Section 1.1 Concerted rearrangement; 1.1.1 Alder ene reaction; 1.1.2 Claisen and related rearrangements; 1.1.3 Cope and related rearrangements; 1.1.4 Curtius rearrangement; 1.1.5 Hofmann rearrangement; 1.1.6 Lossen rearrangement; 1.1.7 Overman rearrangement; 1.1.8 [ 1,2]-Wittig rearrangement; 1.1.9 [2,3]-Wittig rearrangement; 1.1.10 Wolff rearrangement; Section 1.2 Cationic rearrangement; 1.2.1 Beckmann rearrangement; 1.2.2 Demjanov rearrangement
1.2.3 Meyer-Schuster rearrangement1.2.4 Pinacol rearrangement; 1.2.5 Pummerer rearrangement; 1.2.6 Schmidt rearrangement; 1.2.7 Wagner-Meerwein rearrangement; Section 1.3 Anionic rearrangement; 1.3.1 Benzilic acid rearrangement; 1.3.2 Brook rearrangement; 1.3.3 Favorskii rearrangement; 1.3.4 Grob fragmentation; 1.3.5 Neber rearrangement; 1.3.6 Payne rearrangement; 1.3.7 Smiles rearrangement; 1.3.8 Stevens rearrangement; Chapter 2. Asymmetric C-C bond formation; 2.1 Evans aldol reaction; 2.2 Hajos-Wiechert reaction; 2.3 Keck stereoselective allylation; 2.4 Roush allylboronation Chapter 3. Miscellaneous homologation reactions3.1 Bamford-Stevens reaction; 3.2 Mannich reaction; 3.3 Mitsunobu reaction; 3.4 Parham cyclization; 3.5 Passerini reaction; 3.6 Ugi 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 5: Name Reactions for Ring Formations Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-IISubject index |
| Record Nr. | UNINA-9910830941703321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 1 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (733 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| ISBN |
1-282-13765-4
9786612137655 0-470-48702-X 0-470-48701-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part I; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Organometallics; Section 1.1 Palladium Chemistry; 1.1.1 Heck reaction; 1.1.2 Hiyama cross-coupling reaction; 1.1.3 Kumada cross-coupling reaction; 1.1.4 Negishi cross-coupling reaction; 1.1.5 Sonogashira reaction; 1.1.6 Stille coupling; 1.1.7 Suzuki coupling; 1.1.8 Tsuji-Trost reaction; Section 1.2 Organocopper Reagents; 1.2.1 Castro-Stephens coupling; 1.2.2 Glaser coupling; 1.2.3 Ullmann reaction; Section 1.3 Other Organometallic Reagents; 1.3.1 McMurry coupling
1.3.2 Nicholas reaction1.3.3 Nozaki-Hiyama-Kishi reaction; 1.3.4 Tebbe olefination; Chapter 2. Carbon-Chain Homologations; 2.1 Arndt-Eistert homologation; 2.2 Morita-Baylis-Hillman reaction; 2.3 Benzoin condensation; 2.4 Corey-Fuchs reaction; 2.5 Henry reaction; 2.6 Horner-Wadsworth-Emmons reaction; 2.7 Julia-Lythgoe olefination; 2.8 Knoevenagel condensation; 2.9 Mukaiyama aldol reaction; 2.10 Peterson olefination; 2.11 Sakurai allylation reaction; 2.12 Stetter reaction; 2.13 Wittig reaction; Chapter 3. Radical Chemistry; 3.1 Barton-McCombie deoxygenation; 3.2 Barton nitrite photolysis 3.3 Sandmeyer reaction3.4 Wohl-Ziegler 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 4: Name Reactions for Homologations-2; Appendix 4, Table of Contents for Volume 5: Name Reactions for Ring Formations; Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-II; Subject index |
| Record Nr. | UNINA-9910840576103321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey
| Name reactions for homologations . Part 2 [[electronic resource] /] / edited by Jie Jack Li ; foreword by E. J. Corey |
| Pubbl/distr/stampa | Hoboken, : Wiley, c2009 |
| Descrizione fisica | 1 online resource (874 p.) |
| Disciplina |
541.39
547/.2 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Name reactions for homologations |
| Soggetto topico |
Organic compounds - Synthesis
Chemical reactions Chemical tests and reagents |
| ISBN |
1-282-11462-X
9786612114625 0-470-48704-6 0-470-48703-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions for Homologations: Part II; Foreword; Preface; Contributing Authors; Table of Contents; Chapter 1. Rearrangements; Section 1.1 Concerted rearrangement; 1.1.1 Alder ene reaction; 1.1.2 Claisen and related rearrangements; 1.1.3 Cope and related rearrangements; 1.1.4 Curtius rearrangement; 1.1.5 Hofmann rearrangement; 1.1.6 Lossen rearrangement; 1.1.7 Overman rearrangement; 1.1.8 [ 1,2]-Wittig rearrangement; 1.1.9 [2,3]-Wittig rearrangement; 1.1.10 Wolff rearrangement; Section 1.2 Cationic rearrangement; 1.2.1 Beckmann rearrangement; 1.2.2 Demjanov rearrangement
1.2.3 Meyer-Schuster rearrangement1.2.4 Pinacol rearrangement; 1.2.5 Pummerer rearrangement; 1.2.6 Schmidt rearrangement; 1.2.7 Wagner-Meerwein rearrangement; Section 1.3 Anionic rearrangement; 1.3.1 Benzilic acid rearrangement; 1.3.2 Brook rearrangement; 1.3.3 Favorskii rearrangement; 1.3.4 Grob fragmentation; 1.3.5 Neber rearrangement; 1.3.6 Payne rearrangement; 1.3.7 Smiles rearrangement; 1.3.8 Stevens rearrangement; Chapter 2. Asymmetric C-C bond formation; 2.1 Evans aldol reaction; 2.2 Hajos-Wiechert reaction; 2.3 Keck stereoselective allylation; 2.4 Roush allylboronation Chapter 3. Miscellaneous homologation reactions3.1 Bamford-Stevens reaction; 3.2 Mannich reaction; 3.3 Mitsunobu reaction; 3.4 Parham cyclization; 3.5 Passerini reaction; 3.6 Ugi 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 5: Name Reactions for Ring Formations Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry-IISubject index |
| Record Nr. | UNINA-9910841261903321 |
| Hoboken, : Wiley, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Nitrile oxides, nitrones, and nitronates in organic synthesis [[electronic resource] ] : novel strategies in synthesis / / edited by Henry Feuer
| Nitrile oxides, nitrones, and nitronates in organic synthesis [[electronic resource] ] : novel strategies in synthesis / / edited by Henry Feuer |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2008 |
| Descrizione fisica | 1 online resource (767 p.) |
| Disciplina | 547/.2 |
| Altri autori (Persone) |
FeuerHenry <1912->
TorssellKurt <1926-> |
| Collana | Organic Nitro Chemistry |
| Soggetto topico |
Nitrogen oxides
Organic compounds - Synthesis |
| ISBN |
1-281-20380-7
9786611203801 0-470-19155-4 0-470-19154-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | NITRILE OXIDES, NITRONES, AND NITRONATES IN ORGANIC SYNTHESIS; CONTENTS; Series Foreword; List of Abbreviations; 1 Nitrile Oxides; 2 Nitrones: Novel Strategies in Synthesis; 3 Nitronates; Index |
| Record Nr. | UNINA-9910144284303321 |
| Hoboken, N.J., : Wiley-Interscience, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
