Oxidative cross-coupling reactions:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Weinheim, Germany
Wiley-VCH
2016
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| Schlagworte: | |
| Online-Zugang: | FRO01 UBG01 Volltext |
| Beschreibung: | 1 online resource |
| ISBN: | 9783527680986 3527680985 9783527681013 3527681019 |
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| 505 | 8 | |a Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te | |
| 505 | 8 | |a 2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition | |
| 505 | 8 | |a 3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles | |
| 505 | 8 | |a 3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling | |
| 505 | 8 | |a 3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation | |
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Datensatz im Suchindex
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| author | Lei, Aiwen |
| author_facet | Lei, Aiwen |
| author_role | aut |
| author_sort | Lei, Aiwen |
| author_variant | a l al |
| building | Verbundindex |
| bvnumber | BV043864645 |
| collection | ZDB-35-WIC |
| contents | Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te 2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition 3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles 3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling 3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation |
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| indexdate | 2024-07-10T07:37:06Z |
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| publisher | Wiley-VCH |
| record_format | marc |
| spelling | Lei, Aiwen aut Oxidative cross-coupling reactions Aiwen Lei [and 5 others] Weinheim, Germany Wiley-VCH 2016 1 online resource txt rdacontent c rdamedia cr rdacarrier Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te 2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition 3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles 3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling 3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation SCIENCE / Chemistry / Physical & Theoretical bisacsh Chemical reactions fast Nucleophilic reactions fast Oxidation fast Chemie Nucleophilic reactions Chemical reactions Oxidation Kreuzkupplungsreaktion (DE-588)1033635499 gnd rswk-swf Oxidative Kupplungsreaktion (DE-588)4308475-8 gnd rswk-swf Electronic books Kreuzkupplungsreaktion (DE-588)1033635499 s Oxidative Kupplungsreaktion (DE-588)4308475-8 s 1\p DE-604 https://onlinelibrary.wiley.com/doi/book/10.1002/9783527680986 Verlag URL des Erstveröffentlichers Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Lei, Aiwen Oxidative cross-coupling reactions Cover; Title Page; Copyright; Contents; Chapter 1 Oxidative Coupling-Bonding between Two Nucleophiles; 1.1 Introduction/General; 1.1.1 What is Oxidative Cross-Coupling?; 1.1.2 Why Oxidative Cross-Coupling?; 1.1.3 How Does Oxidative Cross-Coupling Work?; 1.1.4 Development and Outlook; References; Chapter 2 Organometals as Nucleophiles; 2.1 Classification and Applications of Organometallic Reagents; 2.2 Csp-M and Csp-M as Nucleophiles; 2.2.1 Alkyne-Alkyne Oxidative Coupling; 2.2.1.1 Alkynyl-Si; 2.2.1.2 Alkynyl-Sn; 2.2.1.3 Alkynyl-B; 2.2.1.4 Alkynyl-Mg; 2.2.1.5 Alkynyl-Te 2.2.2 Alkyne-Cyano Oxidative Coupling2.3 Csp-M and Csp2-M as Nucleophiles; 2.4 Csp-M and Csp3-M as Nucleophiles; 2.5 Csp2-M and Csp2-M as Nucleophiles; 2.5.1 Homocoupling of Csp2-M; 2.5.2 Cross-Coupling between Different Species of Csp2-M; 2.6 Csp2-M and Csp3-M as Nucleophiles; 2.7 Csp3-M and Csp3-M as Nucleophiles; 2.8 Conclusions; References; Chapter 3 Oxidative Couplings Involving the Cleavage of C-H Bonds; 3.1 Theoretical Understandings and Methods in C-H Bond Functionalization; 3.1.1 Introduction; 3.1.2 Mechanisms of C-H Cleavage by Transition Metals; 3.1.2.1 Oxidative Addition 3.1.2.2 Electrophilic Substitution3.1.2.3 -Bond Metathesis; 3.1.2.4 Concerted Metalation Deprotonation (CMD); 3.1.2.5 1,2-Addition; 3.1.2.6 Biomimetic C-H Oxidation; 3.1.2.7 Carbenoid/Nitrenoid C-H Insertion; 3.1.3 Methods for Selective C-H Bond Functionalization; 3.1.3.1 Directed C-H Functionalization; 3.1.3.2 Sterically Controlled C-H Functionalization; 3.1.3.3 C-H Functionalization via Ionic Intermediates; 3.1.3.4 C-H Functionalization via Radical Intermediates; 3.2 Oxidative Couplings between Organometals and Hydrocarbons; 3.2.1 C(sp)-H and Organometals as Nucleophiles 3.2.2 Csp2-H and Organometals as Nucleophiles3.2.3 Csp3-H and Organometals as Nucleophiles; 3.3 Oxidative Couplings between Two Hydrocarbons; 3.3.1 C(sp)-H and C(sp)-H as Nucleophiles; 3.3.2 C(sp)-H and C(sp2)-H as Nucleophiles; 3.3.3 C(sp)-H and C(sp3)-H as Nucleophiles; 3.3.4 Csp2-H and Csp2-H as Nucleophiles; 3.3.4.1 Oxidative Coupling between Directing-Group-Containing Arenes and Unactivated Arenes; 3.3.4.2 Oxidative Coupling of Arenes without Directing Groups; 3.3.4.3 Intramolecular Oxidative Coupling of Unactivated Arenes; 3.3.4.4 Oxidative Heck-Type Cross-Coupling 3.3.5 Csp2-H and Csp3-H as Nucleophiles3.3.5.1 Intramolecular Oxidative Coupling between Aromatic Csp2-H and Csp3-H; 3.3.5.2 Intramolecular Oxidative Coupling between Alkene Csp2-H and Csp3-H; 3.3.5.3 Intermolecular Oxidative Coupling between Csp2-H and Csp3-H; 3.3.6 C(sp3)-H and C(sp3)-H as Nucleophiles; 3.4 Conclusions; References; Chapter 4 Bonding Including Heteroatoms via Oxidative Coupling; 4.1 Introduction; 4.2 Oxidative C-O Bond Formation; 4.2.1 C-H and O-M as Nucleophiles; 4.2.2 C-H and O-H as Nucleophiles; 4.2.2.1 C(sp2, Aryl)-O Bond Formation SCIENCE / Chemistry / Physical & Theoretical bisacsh Chemical reactions fast Nucleophilic reactions fast Oxidation fast Chemie Nucleophilic reactions Chemical reactions Oxidation Kreuzkupplungsreaktion (DE-588)1033635499 gnd Oxidative Kupplungsreaktion (DE-588)4308475-8 gnd |
| subject_GND | (DE-588)1033635499 (DE-588)4308475-8 |
| title | Oxidative cross-coupling reactions |
| title_auth | Oxidative cross-coupling reactions |
| title_exact_search | Oxidative cross-coupling reactions |
| title_full | Oxidative cross-coupling reactions Aiwen Lei [and 5 others] |
| title_fullStr | Oxidative cross-coupling reactions Aiwen Lei [and 5 others] |
| title_full_unstemmed | Oxidative cross-coupling reactions Aiwen Lei [and 5 others] |
| title_short | Oxidative cross-coupling reactions |
| title_sort | oxidative cross coupling reactions |
| topic | SCIENCE / Chemistry / Physical & Theoretical bisacsh Chemical reactions fast Nucleophilic reactions fast Oxidation fast Chemie Nucleophilic reactions Chemical reactions Oxidation Kreuzkupplungsreaktion (DE-588)1033635499 gnd Oxidative Kupplungsreaktion (DE-588)4308475-8 gnd |
| topic_facet | SCIENCE / Chemistry / Physical & Theoretical Chemical reactions Nucleophilic reactions Oxidation Chemie Kreuzkupplungsreaktion Oxidative Kupplungsreaktion |
| url | https://onlinelibrary.wiley.com/doi/book/10.1002/9783527680986 |
| work_keys_str_mv | AT leiaiwen oxidativecrosscouplingreactions |