![Redox‐Active NOx Ligands in Palladium‐Mediated Processes - Fairlamb - 2015 - Angewandte Chemie International Edition - Wiley Online Library Redox‐Active NOx Ligands in Palladium‐Mediated Processes - Fairlamb - 2015 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d6714606-fd8c-455f-b4b9-424d6d987d92/msch001.jpg)
Redox‐Active NOx Ligands in Palladium‐Mediated Processes - Fairlamb - 2015 - Angewandte Chemie International Edition - Wiley Online Library
![Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ... Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/adc21a14-e0fa-48b3-8300-c9711cba22e1/mcontent.jpg)
Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...
![Halide and pseudohalide effects in Pd-catalysed cross-coupling reactions - New Journal of Chemistry (RSC Publishing) DOI:10.1039/B605699G Halide and pseudohalide effects in Pd-catalysed cross-coupling reactions - New Journal of Chemistry (RSC Publishing) DOI:10.1039/B605699G](https://pubs.rsc.org/image/article/2006/NJ/b605699g/b605699g-p1.gif)
Halide and pseudohalide effects in Pd-catalysed cross-coupling reactions - New Journal of Chemistry (RSC Publishing) DOI:10.1039/B605699G
![Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ... Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/f5e6e7b6-5ce0-4958-a268-6da39f682764/mfig001.gif)
Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...
![Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ... Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/f4bf86d1-8032-489d-b693-0c6c7468028d/mfig007.gif)
Exploiting Noninnocent (E,E)‐Dibenzylideneacetone (dba) Effects in Palladium(0)‐Mediated Cross‐Coupling Reactions: Modulation of the Electronic Properties of dba Affects Catalyst Activity and Stability in Ligand and Ligand‐Free Reaction Systems ...
![Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/fb3b757f-bf15-42fb-9a96-4d4f2a7f0e80/mscheme61.gif)
Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library
![π-Acidic alkene ligand effects in Pd-catalysed cross-coupling processes: exploiting the interaction of dibenzylidene acetone (dba) and related ligand ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B811772A π-Acidic alkene ligand effects in Pd-catalysed cross-coupling processes: exploiting the interaction of dibenzylidene acetone (dba) and related ligand ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B811772A](https://pubs.rsc.org/image/article/2008/OB/b811772a/b811772a-s6.gif)
π-Acidic alkene ligand effects in Pd-catalysed cross-coupling processes: exploiting the interaction of dibenzylidene acetone (dba) and related ligand ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B811772A
![Analysis of Stereochemical Convergence in Asymmetric Pd‐Catalysed Allylic Alkylation Reactions Complicated by Halide and Memory Effects - Fairlamb - 2002 - Chemistry – A European Journal - Wiley Online Library Analysis of Stereochemical Convergence in Asymmetric Pd‐Catalysed Allylic Alkylation Reactions Complicated by Halide and Memory Effects - Fairlamb - 2002 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/48cc561d-def8-494e-9cd3-4ca9a4c68d91/msch001.jpg)
Analysis of Stereochemical Convergence in Asymmetric Pd‐Catalysed Allylic Alkylation Reactions Complicated by Halide and Memory Effects - Fairlamb - 2002 - Chemistry – A European Journal - Wiley Online Library
![AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC09810B AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC09810B](https://pubs.rsc.org/image/article/2015/CC/c4cc09810b/c4cc09810b-f2_hi-res.gif)
AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC09810B
![Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/8f4910a4-ef37-4dd6-a0a2-786f76ec3454/mscheme37.gif)
Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library
![Figure 15 from The elusive structure of Pd2(dba)3. Examination by isotopic labeling, NMR spectroscopy, and X-ray diffraction analysis: synthesis and characterization of Pd2(dba-Z)3 complexes. | Semantic Scholar Figure 15 from The elusive structure of Pd2(dba)3. Examination by isotopic labeling, NMR spectroscopy, and X-ray diffraction analysis: synthesis and characterization of Pd2(dba-Z)3 complexes. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/737af48ab24f0d7ff5b8b662613335a752d669ed/9-Figure15-1.png)
Figure 15 from The elusive structure of Pd2(dba)3. Examination by isotopic labeling, NMR spectroscopy, and X-ray diffraction analysis: synthesis and characterization of Pd2(dba-Z)3 complexes. | Semantic Scholar
![Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library Palladium‐Catalysed Cross‐Coupling and Related Processes: Some Interesting Observations That Have Been Exploited in Synthetic Chemistry - McGlacken - 2009 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/f20e21de-eca0-4aba-912f-68af093301e3/mscheme34.gif)