![Pharmaceuticals | Free Full-Text | Synthesis, Antiproliferative Activity, and DNA Binding Studies of Nucleoamino Acid-Containing Pt(II) Complexes | HTML Pharmaceuticals | Free Full-Text | Synthesis, Antiproliferative Activity, and DNA Binding Studies of Nucleoamino Acid-Containing Pt(II) Complexes | HTML](https://www.mdpi.com/pharmaceuticals/pharmaceuticals-13-00284/article_deploy/html/images/pharmaceuticals-13-00284-sch001.png)
Pharmaceuticals | Free Full-Text | Synthesis, Antiproliferative Activity, and DNA Binding Studies of Nucleoamino Acid-Containing Pt(II) Complexes | HTML
![Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.2c00007/asset/images/medium/om2c00007_0011.gif)
Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics
![Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.2c00007/asset/images/large/om2c00007_0006.jpeg)
Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics
![PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes](https://www.researchgate.net/publication/360391796/figure/fig1/AS:1156769778806785@1652806815109/Molecular-structures-of-complexes-1-4-5-and-7-showing-50-probability-ellipsoids_Q320.jpg)
PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes
![Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X20304435-sc1.jpg)
Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect
![Catalytic filtration: efficient C-C cross-coupling using Pd (II) -salen complex-embedded cellulose filter paper as a portable catalyst - RSC Advances (RSC Publishing) DOI:10.1039/D2RA03440A Catalytic filtration: efficient C-C cross-coupling using Pd (II) -salen complex-embedded cellulose filter paper as a portable catalyst - RSC Advances (RSC Publishing) DOI:10.1039/D2RA03440A](https://pubs.rsc.org/image/article/2022/RA/d2ra03440a/d2ra03440a-s1_hi-res.gif)
Catalytic filtration: efficient C-C cross-coupling using Pd (II) -salen complex-embedded cellulose filter paper as a portable catalyst - RSC Advances (RSC Publishing) DOI:10.1039/D2RA03440A
![Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X20304435-gr1.jpg)
Palladium(II) complexes of coumarin substituted 1,2,4–triazol–5–ylidenes for catalytic C–C cross–coupling and C–H activation reactions - ScienceDirect
![Palladium- and Platinum-Catalyzed Addition of Aldehydes and Imines with Allylstannanes. Chemoselective Allylation of Imines in the Presence of Aldehydes | Journal of the American Chemical Society Palladium- and Platinum-Catalyzed Addition of Aldehydes and Imines with Allylstannanes. Chemoselective Allylation of Imines in the Presence of Aldehydes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja9608858/asset/images/medium/ja9608858fb07d.gif)
Palladium- and Platinum-Catalyzed Addition of Aldehydes and Imines with Allylstannanes. Chemoselective Allylation of Imines in the Presence of Aldehydes | Journal of the American Chemical Society
![PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes](https://www.researchgate.net/publication/360391796/figure/fig5/AS:1156769778806787@1652806815306/Syntheses-of-cationic-dicarbene-complexes-8-14-bearing-labile-acetonitrile-co-ligands_Q320.jpg)
PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes
![Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-018-03617-x/MediaObjects/41467_2018_3617_Fig2_HTML.jpg)
Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications
![Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-018-03617-x/MediaObjects/41467_2018_3617_Fig3_HTML.jpg)
Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications
![Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0277538713001459-gr1.jpg)
Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect
![The kinetics and mechanism of polymer‐based NHC‐Pd‐pyridine catalyzed heterogeneous Suzuki reaction in aqueous media - Boztepe - 2019 - International Journal of Chemical Kinetics - Wiley Online Library The kinetics and mechanism of polymer‐based NHC‐Pd‐pyridine catalyzed heterogeneous Suzuki reaction in aqueous media - Boztepe - 2019 - International Journal of Chemical Kinetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/ceef987d-c6d6-4ea2-a9fe-cfbd94bbdb9a/kin21321-fig-0014-m.jpg)
The kinetics and mechanism of polymer‐based NHC‐Pd‐pyridine catalyzed heterogeneous Suzuki reaction in aqueous media - Boztepe - 2019 - International Journal of Chemical Kinetics - Wiley Online Library
![Revealing the Influence of Diverse Secondary Metal Cations on Redox‐Active Palladium Complexes - Golwankar - 2022 - Chemistry – A European Journal - Wiley Online Library Revealing the Influence of Diverse Secondary Metal Cations on Redox‐Active Palladium Complexes - Golwankar - 2022 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/591e33c2-f6c2-44f4-9f97-af346d16d628/chem202200344-toc-0001-m.jpg)
Revealing the Influence of Diverse Secondary Metal Cations on Redox‐Active Palladium Complexes - Golwankar - 2022 - Chemistry – A European Journal - Wiley Online Library
Di-Palladium Complexes are Active Catalysts for Mono-N-Protected Amino Acid-Accelerated Enantioselective C–H Functionalization | ACS Catalysis
Bis(imino)acenaphthene (BIAN)-Supported N-Heterocyclic Carbene Palladium Complexes with Ancillary Ligands: Readily Activated Precatalysts for Direct C–H Arylation of Thiophenes | Organometallics
![Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0277538713001459-fx1.jpg)
Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air - ScienceDirect
![Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-018-03617-x/MediaObjects/41467_2018_3617_Fig1_HTML.jpg)
Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications
![PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes PDF) Palladium hetero‐di(N‐heterocyclic carbene) complexes and their catalytic activities in direct C−H arylation of heteroarenes](https://www.researchgate.net/publication/360391796/figure/fig2/AS:1156769778802695@1652806815157/Comparison-of-Pd-Br-bond-distances-in-hetero-dicarbene-PdII-complexes-I-and-II_Q320.jpg)