Tailored Cationic Palladium( 11) Compounds as Catalysts for Highly Selective Dimerization and Polymerization of Vinylic Monomers
![Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst | Nature Communications Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-019-11838-x/MediaObjects/41467_2019_11838_Fig1_HTML.png)
Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst | Nature Communications
![Table 2 from The air-stable carbocation salt [(MeOC6H4)CPh2][BF4] in Lewis acid catalyzed hydrothiolation of alkenes. | Semantic Scholar Table 2 from The air-stable carbocation salt [(MeOC6H4)CPh2][BF4] in Lewis acid catalyzed hydrothiolation of alkenes. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a6907c824f2033c2744d5d7f554a45f911d8dffc/2-Table2-1.png)
Table 2 from The air-stable carbocation salt [(MeOC6H4)CPh2][BF4] in Lewis acid catalyzed hydrothiolation of alkenes. | Semantic Scholar
![Chiral Anion Directed Asymmetric Carbocation‐Catalyzed Diels–Alder Reactions - Eur. J. Org. Chem. - X-MOL Chiral Anion Directed Asymmetric Carbocation‐Catalyzed Diels–Alder Reactions - Eur. J. Org. Chem. - X-MOL](https://xpic.x-mol.com/thesis%2FEuropean_Journal_of_Organic_Chemistry%2F1bed24b07e250e6bcc9a64d3759b7c443a628609.jpg)
Chiral Anion Directed Asymmetric Carbocation‐Catalyzed Diels–Alder Reactions - Eur. J. Org. Chem. - X-MOL
![Organopalladium Chemistry - Palladium-catalysed nucleophilic allylic substitution of functionalised compounds Organopalladium Chemistry - Palladium-catalysed nucleophilic allylic substitution of functionalised compounds](https://www.chemtube3d.com/images/allylicreactionfinal.png)
Organopalladium Chemistry - Palladium-catalysed nucleophilic allylic substitution of functionalised compounds
![In(OTf)3‐Catalyzed Highly Chemo‐ and Regioselective Head‐to‐Tail Heterodimerization of Vinylarenes with 1,1‐Diarylethenes - Dai - 2011 - Chemistry – A European Journal - Wiley Online Library In(OTf)3‐Catalyzed Highly Chemo‐ and Regioselective Head‐to‐Tail Heterodimerization of Vinylarenes with 1,1‐Diarylethenes - Dai - 2011 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/a24e0315-6175-4ab8-8782-4c5d7c640138/mcontent.gif)
In(OTf)3‐Catalyzed Highly Chemo‐ and Regioselective Head‐to‐Tail Heterodimerization of Vinylarenes with 1,1‐Diarylethenes - Dai - 2011 - Chemistry – A European Journal - Wiley Online Library
![Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species,The Journal of Organic Chemistry - X-MOL Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species,The Journal of Organic Chemistry - X-MOL](https://xpic.x-mol.com/20180410%2F10.1021_acs.joc.8b00331.jpg)
Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species,The Journal of Organic Chemistry - X-MOL
![Stereoselective Reactions with Stabilized Carbocations - Cozzi - 2010 - Angewandte Chemie International Edition - Wiley Online Library Stereoselective Reactions with Stabilized Carbocations - Cozzi - 2010 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/afff1155-2be7-45a3-bcbf-558b444adec8/mcontent.gif)
Stereoselective Reactions with Stabilized Carbocations - Cozzi - 2010 - Angewandte Chemie International Edition - Wiley Online Library
![Insight into the shift and rearrangement of carbocation in Friedel-Crafts alkylation of unsaturated fatty acids revealed by GC–MS - ScienceDirect Insight into the shift and rearrangement of carbocation in Friedel-Crafts alkylation of unsaturated fatty acids revealed by GC–MS - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1387380616302147-sc2.jpg)
Insight into the shift and rearrangement of carbocation in Friedel-Crafts alkylation of unsaturated fatty acids revealed by GC–MS - ScienceDirect
![Theoretical Study of the BF3-Promoted Rearrangement of Oxiranyl N-Methyliminodiacetic Acid Boronates,The Journal of Organic Chemistry - X-MOL Theoretical Study of the BF3-Promoted Rearrangement of Oxiranyl N-Methyliminodiacetic Acid Boronates,The Journal of Organic Chemistry - X-MOL](https://xpic.x-mol.com/20170523%2F10.1021_acs.joc.7b01096.jpg)