Module 1 : Oxidation Reactions Lecture 11 : Other Nonmetal Oxidants (IBX and DDQ) 1 2 3 4 5 · 1.9.5.2 Aromatization DDQ is an effective reagent for the dehydrogenation of hydroaromatic compounds to give aromatic compounds. The procedure can be ...
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Replacement of Stoichiometric DDQ with a Low Potential o-Quinone Catalyst Enabling Aerobic Dehydrogenation of Tertiary Indolines in Pharmaceutical Intermediates. - Abstract - Europe PMC
Reaction-activated palladium catalyst for dehydrogenation of substituted cyclohexanones to phenols and H2 without oxidants and h
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Plausible mechanism of the one-pot multi-component synthesis of flavan... | Download Scientific Diagram
Module 1 : Oxidation Reactions Lecture 11 : Other Nonmetal Oxidants (IBX and DDQ) 1 2 3 4 5 · 1.9.5.2 Aromatization DDQ is an effective reagent for the dehydrogenation of hydroaromatic compounds to give aromatic compounds. The procedure can be ...
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DDQ-mediated regioselective C–S bond formation: efficient access to allylic sulfides - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C8QO00799C
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A practical Δ1-dehydrogenation of Δ4-3-keto-steroids with DDQ in the presence of TBDMSCl at room temperature - ScienceDirect
DDQ-Promoted Mild and Efficient Metal-Free Oxidative -Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
![A practical Δ1-dehydrogenation of Δ4-3-keto-steroids with DDQ in the presence of TBDMSCl at room temperature - ScienceDirect A practical Δ1-dehydrogenation of Δ4-3-keto-steroids with DDQ in the presence of TBDMSCl at room temperature - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0039128X1000070X-sc1.jpg)
A practical Δ1-dehydrogenation of Δ4-3-keto-steroids with DDQ in the presence of TBDMSCl at room temperature - ScienceDirect
![Replacement of Stoichiometric DDQ with a Low Potential o-Quinone Catalyst Enabling Aerobic Dehydrogenation of Tertiary Indolines in Pharmaceutical Intermediates. - Abstract - Europe PMC Replacement of Stoichiometric DDQ with a Low Potential o-Quinone Catalyst Enabling Aerobic Dehydrogenation of Tertiary Indolines in Pharmaceutical Intermediates. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6413530/bin/nihms-1012106-f0005.jpg)
Replacement of Stoichiometric DDQ with a Low Potential o-Quinone Catalyst Enabling Aerobic Dehydrogenation of Tertiary Indolines in Pharmaceutical Intermediates. - Abstract - Europe PMC
DDQ-promoted dehydrogenation from natural rigid polycyclic acids or flexible alkyl acids to generate lactones by a radical ion mechanism - Chemical Communications (RSC Publishing)
![Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML](https://www.mdpi.com/molecules/molecules-13-03236/article_deploy/html/images/molecules-13-03236-g005-550.jpg)
Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML
Oxidative functionalization of benzylic C–H bonds by DDQ - New Journal of Chemistry (RSC Publishing)
![PDF) Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 PDF) Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2](https://www.researchgate.net/publication/23686059/figure/fig1/AS:341843523981325@1458513255549/The-studied-benzoquinones-and-anthraquinones_Q320.jpg)
PDF) Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2
![DDQ-promoted dehydrogenation from natural rigid polycyclic acids or flexible alkyl acids to generate lactones by a radical ion mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C1CC11633A DDQ-promoted dehydrogenation from natural rigid polycyclic acids or flexible alkyl acids to generate lactones by a radical ion mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C1CC11633A](https://pubs.rsc.org/image/article/2011/CC/c1cc11633a/c1cc11633a-s2.gif)
DDQ-promoted dehydrogenation from natural rigid polycyclic acids or flexible alkyl acids to generate lactones by a radical ion mechanism - Chemical Communications (RSC Publishing) DOI:10.1039/C1CC11633A
![Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML](https://www.mdpi.com/molecules/molecules-13-03236/article_deploy/html/images/molecules-13-03236-g001.png)
Molecules | Free Full-Text | Organocatalytic Oxidative Dehydrogenation of Dihydroarenes by Dioxygen Using 2,3-Dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 | HTML
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