![A Mechanistic Investigation of the Kinetic Resolution of Secondary Aromatic Alcohols Using a Ferrocene‐Based Planar Chiral 4‐(Dimethylamino)pyridine Catalyst - Mesas‐Sánchez - 2015 - Chemistry – A European Journal - Wiley Online Library A Mechanistic Investigation of the Kinetic Resolution of Secondary Aromatic Alcohols Using a Ferrocene‐Based Planar Chiral 4‐(Dimethylamino)pyridine Catalyst - Mesas‐Sánchez - 2015 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/fb0c1064-6229-469b-b90a-fbc3b812563b/msch001.jpg)
A Mechanistic Investigation of the Kinetic Resolution of Secondary Aromatic Alcohols Using a Ferrocene‐Based Planar Chiral 4‐(Dimethylamino)pyridine Catalyst - Mesas‐Sánchez - 2015 - Chemistry – A European Journal - Wiley Online Library
![Polymers | Free Full-Text | Recent Advances in the Synthesis and Application of Polymer Compartments for Catalysis | HTML Polymers | Free Full-Text | Recent Advances in the Synthesis and Application of Polymer Compartments for Catalysis | HTML](https://www.mdpi.com/polymers/polymers-12-02190/article_deploy/html/images/polymers-12-02190-g005.png)
Polymers | Free Full-Text | Recent Advances in the Synthesis and Application of Polymer Compartments for Catalysis | HTML
![Chapter 1 Nucleophilic Catalysts and Organocatalyzed Zwitterionic Ring-opening Polymerization of Heterocyclic Monomers (RSC Publishing) DOI:10.1039/9781788015738-00001 Chapter 1 Nucleophilic Catalysts and Organocatalyzed Zwitterionic Ring-opening Polymerization of Heterocyclic Monomers (RSC Publishing) DOI:10.1039/9781788015738-00001](https://pubs.rsc.org/image/chapter/bk9781788011846/bk9781788011846-00001/bk9781788011846-00001-s3_hi-res.gif)
Chapter 1 Nucleophilic Catalysts and Organocatalyzed Zwitterionic Ring-opening Polymerization of Heterocyclic Monomers (RSC Publishing) DOI:10.1039/9781788015738-00001
![Catalysts | Free Full-Text | Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis | HTML Catalysts | Free Full-Text | Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis | HTML](https://www.mdpi.com/catalysts/catalysts-06-00128/article_deploy/html/images/catalysts-06-00128-sch007.png)
Catalysts | Free Full-Text | Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis | HTML
![Scheme 1. Proposed Mechanism for [Cu(MeCN) 4 ]PF 6 / DBED/DMAP Catalyst... | Download Scientific Diagram Scheme 1. Proposed Mechanism for [Cu(MeCN) 4 ]PF 6 / DBED/DMAP Catalyst... | Download Scientific Diagram](https://www.researchgate.net/publication/313971430/figure/fig3/AS:465341852721154@1487957551725/Scheme-1-Proposed-Mechanism-for-CuMeCN-4-PF-6-DBED-DMAP-Catalyst-System.png)
Scheme 1. Proposed Mechanism for [Cu(MeCN) 4 ]PF 6 / DBED/DMAP Catalyst... | Download Scientific Diagram
![Nucleophilic Catalysis by 4‐(Dialkylamino)pyridines Revisited—The Search for Optimal Reactivity and Selectivity - Spivey - 2004 - Angewandte Chemie International Edition - Wiley Online Library Nucleophilic Catalysis by 4‐(Dialkylamino)pyridines Revisited—The Search for Optimal Reactivity and Selectivity - Spivey - 2004 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f961c742-6d48-4375-a309-beeb27b5f99c/mcontent.jpg)
Nucleophilic Catalysis by 4‐(Dialkylamino)pyridines Revisited—The Search for Optimal Reactivity and Selectivity - Spivey - 2004 - Angewandte Chemie International Edition - Wiley Online Library
![Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms11297/MediaObjects/41467_2016_Article_BFncomms11297_Fig1_HTML.jpg)
Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications
![A novel chiral DMAP–thiourea bifunctional catalyst catalyzed enantioselective Steglich and Black rearrangement reactions - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00691E A novel chiral DMAP–thiourea bifunctional catalyst catalyzed enantioselective Steglich and Black rearrangement reactions - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00691E](https://pubs.rsc.org/image/article/2019/QO/c9qo00691e/c9qo00691e-s1_hi-res.gif)
A novel chiral DMAP–thiourea bifunctional catalyst catalyzed enantioselective Steglich and Black rearrangement reactions - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00691E
![Scheme IV.5: Mechanism of activation with DCC using DMAP as a catalyst. | Download Scientific Diagram Scheme IV.5: Mechanism of activation with DCC using DMAP as a catalyst. | Download Scientific Diagram](https://www.researchgate.net/profile/Steven-Van-Der-Plas-2/publication/292609723/figure/fig10/AS:669495962112010@1536631684267/Scheme-IV5-Mechanism-of-activation-with-DCC-using-DMAP-as-a-catalyst.png)
Scheme IV.5: Mechanism of activation with DCC using DMAP as a catalyst. | Download Scientific Diagram
Scheme 1 Mechanism of the formation of E-CNCs with DMAP as a catalyst. | Download Scientific Diagram
![Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/b79a1771-7ab0-4d94-9117-6c481a5d7e98/mcontent.gif)
Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library
![Recent topics in enantioselective acyl transfer reactions with dialkylaminopyridine-based nucleophilic catalysts - ScienceDirect Recent topics in enantioselective acyl transfer reactions with dialkylaminopyridine-based nucleophilic catalysts - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403918303137-gr1.jpg)