Inventing reactions
Barry Trost: Transition metal catalyzed allylic alkylation.- Jeffrey W. Bode: Reinventing Amide Bond Formation.- Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds.- Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Dis...
Gardado en:
| Autor Principal: | |
|---|---|
| Formato: | Livre numérique |
| Idioma: | Anglais |
| Publicado: |
Berlin, Heidelberg :
Springer Berlin Heidelberg
[20..].
Cham : Springer Nature |
| Edición: | 1st ed. 2013. |
| Series: | Topics in Organometallic Chemistry
44 |
| Sujets: | |
| Acceso en liña: | Accès sur la plateforme de l'éditeur Accès sur la plateforme Istex Accès Université d'Orléans Accès INSA CVL |
| Nota: |
Archives Springer e-books (Licence nationale) Archives Springer e-books (Licence nationale) |
| Autres localisations: | Voir dans le Sudoc |
| Edition sous un autre format: | • Inventing Reactions, Texte imprimé, 9783642342875 • Inventing Reactions, Texte imprimé, 9783642448782 • Inventing reactions, volume editor, Lukas J. Gooßen, Berlin, Springer, 2013, 1 vol. (xiv, 340 p.), Topics in organometallic chemistry, 978-3-642-34285-1 |
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| 041 | 0 | |a eng | |
| 082 | |a 541.39 | ||
| 100 | 1 | |a Gooßen, Lukas J. | |
| 245 | 1 | 0 | |a Inventing reactions |c volume Editor : Lukas J. Gooßen ; with contributions by D. C. Behenna, G.L. Beutner, S. M. Bischof, ... [et al.]. |
| 250 | |a 1st ed. 2013. | ||
| 260 | |a Berlin, Heidelberg : |b Springer Berlin Heidelberg. | ||
| 260 | |a Cham : |b Springer Nature, |c [20..]. | ||
| 490 | 0 | |a Topics in Organometallic Chemistry |v 44 |x 1616-8534 | |
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 505 | 1 | |a Barry Trost: Transition metal catalyzed allylic alkylation Jeffrey W. Bode: Reinventing Amide Bond Formation Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis David R. Stuart and Keith Fagnou: The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes Lukas Gooßen and Käthe Gooßen: Decarboxylative Cross-Coupling Reactions A. Stephen K. Hashmi: Gold-Catalyzed Organic Reactions Ben List: Developing Catalytic Asymmetric Acetalizations Steven M. Bischof, Brian G. Hashiguchi, Michael M. Konnick, and Roy A. Periana: The De NovoDesign of CH Bond Hydroxylation Catalysts Benoit Cardinal-David, Karl A. Scheidt: Carbene Catalysis: Beyond the Benzoin and Stetter Reactions Kenso Soai and Tsuneomi Kawasaki: Asymmetric autocatalysis of pyrimidyl alkanol Douglas C. Behenna and Brian M. Stoltz: Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents. Hisashi Yamamoto: Acid Catalysis in Organic Synthesis. | |
| 505 | 0 | |a Content -- Chapitre 1 : Catalysis: Unlimited Frontiers Our Early Personal Journey into the World of Palladium -- Chapitre 2 : Reinventing Amide Bond Formation -- Chapitre 3 : Catalytic Transformations Involving the Cleavage of C-OMe Bonds -- Chapitre 4 : The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis -- Chapitre 5 : The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes -- Chapitre 6 : Decarboxylative Cross-Coupling Reactions -- Chapitre 7 : Gold-Catalyzed Organic Reactions -- Chapitre 8 : Developing Catalytic Asymmetric Acetalizations -- Chapitre 9 : Designing Molecular Catalysts for Selective CH Functionalization -- Chapitre 10 : Carbene Catalysis: Beyond the Benzoin and Stetter Reactions -- Chapitre 11 : Asymmetric autocatalysis of pyrimidyl alkanol -- Chapitre 12 : Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents -- Chapitre 13 : Acid Catalysis in Organic Synthesis | |
| 506 | |a Accès en ligne pour les établissements français bénéficiaires des licences nationales | ||
| 506 | |a Accès soumis à abonnement pour tout autre établissement | ||
| 506 | |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 | ||
| 520 | |a Barry Trost: Transition metal catalyzed allylic alkylation.- Jeffrey W. Bode: Reinventing Amide Bond Formation.- Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds.- Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis.- David R. Stuart and Keith Fagnou: The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes.- Lukas Gooßen and Käthe Gooßen: Decarboxylative Cross-Coupling Reactions.- A. Stephen K. Hashmi: Gold-Catalyzed Organic Reactions.- Ben List: Developing Catalytic Asymmetric Acetalizations.- Steven M. Bischof, Brian G. Hashiguchi, Michael M. Konnick, and Roy A. Periana: The De NovoDesign of CH Bond Hydroxylation Catalysts.- Benoit Cardinal-David, Karl A. Scheidt: Carbene Catalysis: Beyond the Benzoin and Stetter Reactions.- Kenso Soai and Tsuneomi Kawasaki: Asymmetric autocatalysis of pyrimidyl alkanol.- Douglas C. Behenna and Brian M. Stoltz: Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents. Hisashi Yamamoto: Acid Catalysis in Organic Synthesis. | ||
| 650 | |a Réactions chimiques | ||
| 650 | |a Composés organométalliques | ||
| 650 | |a Chimie organométallique | ||
| 650 | |a Catalyse | ||
| 776 | 0 | |t Inventing Reactions |b Texte imprimé |z 9783642342875 | |
| 776 | 0 | |t Inventing Reactions |b Texte imprimé |z 9783642448782 | |
| 776 | 0 | |0 168791404 |t Inventing reactions |f volume editor, Lukas J. Gooßen |c Berlin |n Springer |d 2013 |p 1 vol. (xiv, 340 p.) |s Topics in organometallic chemistry |z 978-3-642-34285-1 | |
| 856 | 4 | |q PDF |u https://doi.org/10.1007/978-3-642-34286-8 |z Accès sur la plateforme de l'éditeur | |
| 856 | 4 | |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-JT727QDG-0 |z Accès sur la plateforme Istex | |
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