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Domino Reactions : Concepts for Efficient Organic Synthesis.
The follow-up to the successful ""Domino Reaction in Organic Synthesis"", this ready reference brings up to date on the original concept. The chapters have been arranged according to the name of well-known transformations of the first step and in combination with the formed produ...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Hoboken :
Wiley,
2013.
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| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000Mi 4500 | ||
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| 003 | OCoLC | ||
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| 049 | |a UAMI | ||
| 100 | 1 | |a Tietze, Lutz F. | |
| 245 | 1 | 0 | |a Domino Reactions : |b Concepts for Efficient Organic Synthesis. |
| 260 | |a Hoboken : |b Wiley, |c 2013. | ||
| 300 | |a 1 online resource (647 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Domino Reactions; Contents; Preface; List of Contributors; List of Abbreviations; Chapter Introduction; References; Chapter 1 Transition-Metal-Catalyzed Carbonylative Domino Reactions; 1.1 Introduction; 1.2 Transition-Metal-Catalyzed Carbonylative Domino Reactions; 1.2.1 Ruthenium-Catalyzed Carbonylative Domino Reactions; 1.2.2 Rhodium-Catalyzed Carbonylative Domino Reactions; 1.2.3 Palladium-Catalyzed Carbonylative Domino Reactions; 1.2.4 Iron-, Copper-, Nickel-, and Cobalt-Catalyzed Carbonylative Domino Reactions; 1.3 Outlook; References; Chapter 2 Metathesis Reactions in Domino Processes. | |
| 505 | 8 | |a 2.1 Domino Processes Featuring Solely Metathesis Events2.1.1 Reactions Involving Only Alkenes; 2.1.2 Reactions Involving Alkenes and Alkynes; 2.2 Domino Processes Featuring Metathesis and Non-metathesis Events; 2.2.1 Metathesis/Redox Transformation; 2.2.2 Metathesis/Isomerization; 2.2.3 Metathesis/Cycloaddition; 2.2.4 Metathesis/Substitution; 2.2.5 Metathesis/Conjugate Addition; 2.2.6 Metathesis/Carbonyl Olefination; 2.3 Conclusion and Outlook; Acknowledgments; References; Chapter 3 C-H Activation Reactions in Domino Processes; 3.1 Heck Reactions/C-H Activations. | |
| 505 | 8 | |a 3.2 Carbopalladations and Aminopalladations of Alkynes/C-H Activations3.3 Palladium-Catalyzed/Norbornene-Mediated ortho C-H Activations; 3.4 Domino Reactions Involving Heteroatom-Directed C-H Activations; 3.5 Conclusions; References; Chapter 4 Domino Reactions Initiated by Nucleophilic Substitution; 4.1 Domino SN/Michael Addition and Related Reactions; 4.2 Domino Reactions Initiated by Nucleophilic Ring Opening of Aziridines, Epoxides, and Activated Cyclopropanes; 4.3 Domino SN/Brook Rearrangements; References; Chapter 5 Radical Reactions in Domino Processes; 5.1 Introduction. | |
| 505 | 8 | |a 5.2 Radical/Cation Domino Processes5.3 Radical/Anionic Domino Processes; 5.4 Domino Radical/Radical Process; 5.5 Radical/Pericyclic Domino Processes; 5.6 Asymmetric Radical Domino Processes; 5.6.1 Chiral Auxiliary-Directed Asymmetric Radical Domino Processes; 5.6.2 Chiral Catalyst-Driven Asymmetric Radical Domino Processes; 5.7 Conclusion and Outlook; Acknowledgments; References; Chapter 6 Pericyclic Reactions in Domino Processes; 6.1 Introduction; 6.2 Cycloadditions; 6.2.1 Cycloaddition/Cycloaddition; 6.2.2 Cycloaddition/Cycloreversion; 6.2.3 Cycloaddition/Sigmatropic Rearrangement. | |
| 505 | 8 | |a 6.2.4 Cycloaddition/Electrocyclization6.2.5 Cycloaddition/Mixed Transformations; 6.3 Sigmatropic Rearrangements; 6.3.1 Sigmatropic Rearrangement/Sigmatropic Rearrangement; 6.3.2 Sigmatropic Rearrangement/Cycloaddition; 6.3.3 Sigmatropic Rearrangement/Electrocyclization; 6.3.4 Sigmatropic Rearrangement/Mixed Transformations; 6.4 Electrocyclizations; 6.4.1 Electrocyclization/Electrocyclization; 6.4.2 Electrocyclization/Cycloaddition; 6.4.3 Electrocyclization/Sigmatropic Rearrangement; 6.4.4 Electrocyclization/Mixed Transformations; 6.5 Mixed Transformations. | |
| 500 | |a 6.5.1 Mixed Transformations Followed by Pericyclic Reactions. | ||
| 520 | |a The follow-up to the successful ""Domino Reaction in Organic Synthesis"", this ready reference brings up to date on the original concept. The chapters have been arranged according to the name of well-known transformations of the first step and in combination with the formed products. Each chapter is written by an internationally renowned expert, and the book is edited by L.F. Tietze, who established the concept of domino reactions. The one-stop source for all synthetic chemists to improve the synthetic efficiency and allow an ecologically and economically beneficial preparation of ev. | ||
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Organic compounds |x Synthesis. | |
| 650 | 6 | |a Composés organiques |x Synthèse. | |
| 650 | 7 | |a Organic compounds |x Synthesis |2 fast | |
| 758 | |i has work: |a Domino reactions (Text) |1 https://id.oclc.org/worldcat/entity/E39PCGkbFBCq99Db3bT9VW7M8C |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |a Tietze, Lutz F. |t Domino Reactions : Concepts for Efficient Organic Synthesis. |d Hoboken : Wiley, ©2013 |z 9783527334322 |
| 856 | 4 | 0 | |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=1584785 |z Texto completo |
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