Palladium-Catalyzed Intramolecular 5-exo-dig Hydroarylations of N-Arylpropiolamides: Thermodynamics-Controlled Stereoselective Synthesis of 3-Methyleneoxindoles | The Journal of Organic Chemistry
![N, O-polydentate ligands for palladium-catalyzed cross-coupling reactions (Part III) - ScienceDirect N, O-polydentate ligands for palladium-catalyzed cross-coupling reactions (Part III) - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X2100468X-ga1.jpg)
N, O-polydentate ligands for palladium-catalyzed cross-coupling reactions (Part III) - ScienceDirect
![Optimization of Levulinic Acid Production from Depithed Sugarcane Bagasse in 1- Ethyl-3-methylimidazolium hydrogen sulfate [EMim][HSO4] | SpringerLink Optimization of Levulinic Acid Production from Depithed Sugarcane Bagasse in 1- Ethyl-3-methylimidazolium hydrogen sulfate [EMim][HSO4] | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12649-020-01221-z/MediaObjects/12649_2020_1221_Figa_HTML.png)
Optimization of Levulinic Acid Production from Depithed Sugarcane Bagasse in 1- Ethyl-3-methylimidazolium hydrogen sulfate [EMim][HSO4] | SpringerLink
![Entropy | Free Full-Text | Reaction Mechanism of CO2 with Choline-Amino Acid Ionic Liquids: A Computational Study Entropy | Free Full-Text | Reaction Mechanism of CO2 with Choline-Amino Acid Ionic Liquids: A Computational Study](https://www.mdpi.com/entropy/entropy-24-01572/article_deploy/html/images/entropy-24-01572-g008.png)
Entropy | Free Full-Text | Reaction Mechanism of CO2 with Choline-Amino Acid Ionic Liquids: A Computational Study
![1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols | ACS Sustainable Chemistry & Engineering 1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols | ACS Sustainable Chemistry & Engineering](https://pubs.acs.org/cms/10.1021/acssuschemeng.8b02614/asset/images/large/sc-2018-02614b_0011.jpeg)
1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols | ACS Sustainable Chemistry & Engineering
![Covalent organic framework supported palladium catalysts - Journal of Materials Chemistry A (RSC Publishing) DOI:10.1039/D2TA05234B Covalent organic framework supported palladium catalysts - Journal of Materials Chemistry A (RSC Publishing) DOI:10.1039/D2TA05234B](https://pubs.rsc.org/image/article/2022/TA/d2ta05234b/d2ta05234b-f4_hi-res.gif)
Covalent organic framework supported palladium catalysts - Journal of Materials Chemistry A (RSC Publishing) DOI:10.1039/D2TA05234B
Mild Palladium-Catalyzed Selective Monoarylation of Nitriles | Journal of the American Chemical Society
![Synthesis of Benzothiophene-3-carboxylic Esters by Palladium Iodide-Catalyzed Oxidative Cyclization–Deprotection–Alkoxycarbonylation Sequence under Aerobic Conditions - ScienceDirect Synthesis of Benzothiophene-3-carboxylic Esters by Palladium Iodide-Catalyzed Oxidative Cyclization–Deprotection–Alkoxycarbonylation Sequence under Aerobic Conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S002232632202240X-jo2c00686_0005.jpg)
Synthesis of Benzothiophene-3-carboxylic Esters by Palladium Iodide-Catalyzed Oxidative Cyclization–Deprotection–Alkoxycarbonylation Sequence under Aerobic Conditions - ScienceDirect
![Structures of acridine derivatives examined for effect on TDP-43 2C... | Download Scientific Diagram Structures of acridine derivatives examined for effect on TDP-43 2C... | Download Scientific Diagram](https://www.researchgate.net/publication/311807331/figure/fig1/AS:442013360365569@1482395606601/Structures-of-acridine-derivatives-examined-for-effect-on-TDP-43-2C-aggregation-AIM1.png)
Structures of acridine derivatives examined for effect on TDP-43 2C... | Download Scientific Diagram
![Trimetallic PEPPSI‐Type Palladium N‐Heterocyclic Carbene Complexes – Improved Catalyst Lifetime in the Mizoroki–Heck Coupling Reaction - Martínez‐Olid - 2015 - European Journal of Inorganic Chemistry - Wiley Online Library Trimetallic PEPPSI‐Type Palladium N‐Heterocyclic Carbene Complexes – Improved Catalyst Lifetime in the Mizoroki–Heck Coupling Reaction - Martínez‐Olid - 2015 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/a2b01b41-2749-4bb6-8078-2d2ab12570c0/mfig000.jpg)
Trimetallic PEPPSI‐Type Palladium N‐Heterocyclic Carbene Complexes – Improved Catalyst Lifetime in the Mizoroki–Heck Coupling Reaction - Martínez‐Olid - 2015 - European Journal of Inorganic Chemistry - Wiley Online Library
![Nonsolvent application of ionic liquids: organo-catalysis by 1-alkyl-3- methylimidazolium cation based room-temperature ionic liquids for chemoselective N-tert-butyloxycarbonylation of amines and the influence of the C-2 hydrogen on catalytic efficiency ... Nonsolvent application of ionic liquids: organo-catalysis by 1-alkyl-3- methylimidazolium cation based room-temperature ionic liquids for chemoselective N-tert-butyloxycarbonylation of amines and the influence of the C-2 hydrogen on catalytic efficiency ...](https://d3i71xaburhd42.cloudfront.net/4fd9b70db8706a4d4b051928fc80c05d8cd36e92/2-Table1-1.png)
Nonsolvent application of ionic liquids: organo-catalysis by 1-alkyl-3- methylimidazolium cation based room-temperature ionic liquids for chemoselective N-tert-butyloxycarbonylation of amines and the influence of the C-2 hydrogen on catalytic efficiency ...
![Palladium-catalyzed ionic liquid-accelerated oxidative annulation of acetylenic oximes with unactivated long-chain enols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC02037K Palladium-catalyzed ionic liquid-accelerated oxidative annulation of acetylenic oximes with unactivated long-chain enols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC02037K](https://pubs.rsc.org/image/article/2020/GC/d0gc02037k/d0gc02037k-s1_hi-res.gif)
Palladium-catalyzed ionic liquid-accelerated oxidative annulation of acetylenic oximes with unactivated long-chain enols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC02037K
![Mild Palladium-Catalyzed Selective Monoarylation of Nitriles | Journal of the American Chemical Society Mild Palladium-Catalyzed Selective Monoarylation of Nitriles | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja053027x/asset/images/medium/ja053027xf2.gif)