![C–H functionalization by high-valent Cp*Co( iii ) catalysis - Chemical Communications (RSC Publishing) DOI:10.1039/C6CC09651D C–H functionalization by high-valent Cp*Co( iii ) catalysis - Chemical Communications (RSC Publishing) DOI:10.1039/C6CC09651D](https://pubs.rsc.org/image/article/2017/CC/c6cc09651d/c6cc09651d-s23_hi-res.gif)
C–H functionalization by high-valent Cp*Co( iii ) catalysis - Chemical Communications (RSC Publishing) DOI:10.1039/C6CC09651D
![A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram](https://www.researchgate.net/publication/337234116/figure/fig3/AS:11431281183083921@1692698943987/Gibbs-free-energy-profile-for-reaction-1-for-the-conventional-monometallic-energies_Q320.jpg)
A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram
Gibbs free energy profile for the concerted metalation–deprotonation... | Download Scientific Diagram
C–H Activation versus Ring Opening and Inner- versus Outer-Sphere Concerted Metalation–Deprotonation in Rh(III)-Catalyzed Ox
![Figure 1 from Investigation of the mechanism of C(sp3)-H bond cleavage in Pd(0)-catalyzed intramolecular alkane arylation adjacent to amides and sulfonamides. | Semantic Scholar Figure 1 from Investigation of the mechanism of C(sp3)-H bond cleavage in Pd(0)-catalyzed intramolecular alkane arylation adjacent to amides and sulfonamides. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/4789d5f47eed1ee385ef73847d1addaaa9b09c00/3-Figure1-1.png)
Figure 1 from Investigation of the mechanism of C(sp3)-H bond cleavage in Pd(0)-catalyzed intramolecular alkane arylation adjacent to amides and sulfonamides. | Semantic Scholar
![Concerted vs Nonconcerted Metalation–Deprotonation in Orthogonal Direct C–H Arylation of Heterocycles with Halides: A Computational Study - ScienceDirect Concerted vs Nonconcerted Metalation–Deprotonation in Orthogonal Direct C–H Arylation of Heterocycles with Halides: A Computational Study - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022326321010252-jo0c02604_0001.jpg)
Concerted vs Nonconcerted Metalation–Deprotonation in Orthogonal Direct C–H Arylation of Heterocycles with Halides: A Computational Study - ScienceDirect
![Relative Strength of Common Directing Groups in Palladium-Catalyzed Aromatic C−H Activation - ScienceDirect Relative Strength of Common Directing Groups in Palladium-Catalyzed Aromatic C−H Activation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2589004219303748-sc2.jpg)
Relative Strength of Common Directing Groups in Palladium-Catalyzed Aromatic C−H Activation - ScienceDirect
![Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism](https://www.mdpi.com/molecules/molecules-26-04083/article_deploy/html/images/molecules-26-04083-g003.png)
Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism
![A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram](https://www.researchgate.net/publication/337234116/figure/fig2/AS:11431281183083915@1692698941677/A-generalized-representation-of-a-concerted-metalation-deprotonation-CMD-and-b_Q320.jpg)
A generalized representation of (a) concerted metalation–deprotonation... | Download Scientific Diagram
![Computational exploration of Pd‐catalyzed C–H bond activation reactions - Yang - 2018 - International Journal of Quantum Chemistry - Wiley Online Library Computational exploration of Pd‐catalyzed C–H bond activation reactions - Yang - 2018 - International Journal of Quantum Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f490d377-b43f-4e0b-8fc9-a5ec65cb724b/qua25723-fig-0009-m.jpg)
Computational exploration of Pd‐catalyzed C–H bond activation reactions - Yang - 2018 - International Journal of Quantum Chemistry - Wiley Online Library
![Oligothiophene Synthesis by a Distinct, General C−H Activation Mechanism: Electrophilic Concerted Metalation-Deprotonation (eCMD) | Catalysis | ChemRxiv | Cambridge Open Engage Oligothiophene Synthesis by a Distinct, General C−H Activation Mechanism: Electrophilic Concerted Metalation-Deprotonation (eCMD) | Catalysis | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c74021702a9b2fef18a054/largeThumb/oligothiophene-synthesis-by-a-distinct-general-c-h-activation-mechanism-electrophilic-concerted-metalation-deprotonation-e-cmd.jpg)
Oligothiophene Synthesis by a Distinct, General C−H Activation Mechanism: Electrophilic Concerted Metalation-Deprotonation (eCMD) | Catalysis | ChemRxiv | Cambridge Open Engage
Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aro
![Figure 1 from Analysis of the concerted metalation-deprotonation mechanism in palladium-catalyzed direct arylation across a broad range of aromatic substrates. | Semantic Scholar Figure 1 from Analysis of the concerted metalation-deprotonation mechanism in palladium-catalyzed direct arylation across a broad range of aromatic substrates. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/4f7b08a0b00d427759c568d1bf80392da85293ca/1-Figure1-1.png)
Figure 1 from Analysis of the concerted metalation-deprotonation mechanism in palladium-catalyzed direct arylation across a broad range of aromatic substrates. | Semantic Scholar
![Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism](https://www.mdpi.com/molecules/molecules-26-04083/article_deploy/html/images/molecules-26-04083-g001.png)
Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism
![Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism](https://pub.mdpi-res.com/molecules/molecules-26-04083/article_deploy/html/images/molecules-26-04083-sch004.png?1625384234)
Molecules | Free Full-Text | The Activating Effect of Strong Acid for Pd-Catalyzed Directed C–H Activation by Concerted Metalation-Deprotonation Mechanism
C–H bond activation via concerted metalation–deprotonation at a palladium(iii) center - Chemical Science (RSC Publishing)
![The mechanism of the Pd-catalyzed formation of coumarins: a theoretical study - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/C4CP03418J The mechanism of the Pd-catalyzed formation of coumarins: a theoretical study - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/C4CP03418J](https://pubs.rsc.org/image/article/2015/CP/c4cp03418j/c4cp03418j-f4_hi-res.gif)
The mechanism of the Pd-catalyzed formation of coumarins: a theoretical study - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/C4CP03418J
![C-H Bond Activation via Concerted Metalation-Deprotonation at a Palladium(III) Center | Organometallic Chemistry | ChemRxiv | Cambridge Open Engage C-H Bond Activation via Concerted Metalation-Deprotonation at a Palladium(III) Center | Organometallic Chemistry | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/63a33573a53ea6cb53532aa4/largeThumb/c-h-bond-activation-via-concerted-metalation-deprotonation-at-a-palladium-iii-center.jpg)
C-H Bond Activation via Concerted Metalation-Deprotonation at a Palladium(III) Center | Organometallic Chemistry | ChemRxiv | Cambridge Open Engage
![NBO Orbital Interaction Analysis for the Ambiphilic Metal–Ligand Activation/Concerted Metalation Deprotonation (AMLA/CMD) Mechanism Involved in the Cyclopalladation Reaction of N,N‑Dimethylbenzylamine with Palladium Acetate - ScienceDirect NBO Orbital Interaction Analysis for the Ambiphilic Metal–Ligand Activation/Concerted Metalation Deprotonation (AMLA/CMD) Mechanism Involved in the Cyclopalladation Reaction of N,N‑Dimethylbenzylamine with Palladium Acetate - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S027673332104053X-om-2018-00303u_0014.jpg)