![p‐toluenesulfonic acid‐catalyzed synthesis of polysubstituted quinolines via Friedländer reaction under ball‐milling conditions at room temperature and theoretical study on the mechanism using a density functional theory method - Javanshir - 2014 - p‐toluenesulfonic acid‐catalyzed synthesis of polysubstituted quinolines via Friedländer reaction under ball‐milling conditions at room temperature and theoretical study on the mechanism using a density functional theory method - Javanshir - 2014 -](https://onlinelibrary.wiley.com/cms/asset/0e05ba33-c5de-44b2-96f4-76a095f7b68f/poc3305-fig-0008-m.jpg)
p‐toluenesulfonic acid‐catalyzed synthesis of polysubstituted quinolines via Friedländer reaction under ball‐milling conditions at room temperature and theoretical study on the mechanism using a density functional theory method - Javanshir - 2014 -
Sciencemadness Discussion Board - ortho nitration of p-toluenesulfonic acid(QUESTIONS) - Powered by XMB 1.9.11
![Illustrated Glossary of Organic Chemistry - Toluenesulfonic acid (p-toluenesulfonic acid; TsOH; p-TsOH) Illustrated Glossary of Organic Chemistry - Toluenesulfonic acid (p-toluenesulfonic acid; TsOH; p-TsOH)](http://www.chem.ucla.edu/~harding/IGOC/T/toluenesulfonic_acid01.png)
Illustrated Glossary of Organic Chemistry - Toluenesulfonic acid (p-toluenesulfonic acid; TsOH; p-TsOH)
![Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink](https://media.springernature.com/full/springer-static/image/art%3A10.1007%2Fs00706-014-1273-y/MediaObjects/706_2014_1273_Figb_HTML.gif)
Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink
![Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo971832r/asset/images/large/jo971832rh00004.jpeg)
Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry
![p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions - ScienceDirect p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403907009240-fx1.jpg)
p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions - ScienceDirect
![Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00706-014-1273-y/MediaObjects/706_2014_1273_Sch1_HTML.gif)
Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink
![organic chemistry - Verify my expected product of two acid/base reactions and does chosen solvent change reaction? - Chemistry Stack Exchange organic chemistry - Verify my expected product of two acid/base reactions and does chosen solvent change reaction? - Chemistry Stack Exchange](https://i.stack.imgur.com/UfjN9.png)
organic chemistry - Verify my expected product of two acid/base reactions and does chosen solvent change reaction? - Chemistry Stack Exchange
![p-Toluenesulfonic acid-catalyzed one-pot synthesis of 2-amino-4-substituted-1,4-dihydrobenzo[4,5]imidazolo[1,2-a]pyrimidine-3-carbonitriles under neat conditions - ScienceDirect p-Toluenesulfonic acid-catalyzed one-pot synthesis of 2-amino-4-substituted-1,4-dihydrobenzo[4,5]imidazolo[1,2-a]pyrimidine-3-carbonitriles under neat conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1631074813002646-sc2.jpg)
p-Toluenesulfonic acid-catalyzed one-pot synthesis of 2-amino-4-substituted-1,4-dihydrobenzo[4,5]imidazolo[1,2-a]pyrimidine-3-carbonitriles under neat conditions - ScienceDirect
![Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo971832r/asset/images/large/jo971832rh00002.jpeg)
Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus | The Journal of Organic Chemistry
![Schematic of the reaction between p-toluenesulfonic acid monohydrate... | Download Scientific Diagram Schematic of the reaction between p-toluenesulfonic acid monohydrate... | Download Scientific Diagram](https://www.researchgate.net/publication/320933728/figure/fig1/AS:558471767695368@1510161453903/Schematic-of-the-reaction-between-p-toluenesulfonic-acid-monohydrate-and-azetidinium-salt.png)
Schematic of the reaction between p-toluenesulfonic acid monohydrate... | Download Scientific Diagram
p-Toluenesulfonic acid functionalized imidazole ionic liquids encapsulated into bismuth SBA-16 as high-efficiency catalysts for Friedel–Crafts acylation reaction - Dalton Transactions (RSC Publishing)
![A facile and practical p-Toluenesulfonic acid catalyzed route to dicoumarols containing an Aroyl group A facile and practical p-Toluenesulfonic acid catalyzed route to dicoumarols containing an Aroyl group](http://www.scielo.org.za/img/revistas/sajc/v68/08s02.jpg)
A facile and practical p-Toluenesulfonic acid catalyzed route to dicoumarols containing an Aroyl group
![Supported p-Toluenesulfonic Acid as a Highly Robust and Eco-Friendly Isocyanide Scavenger | ACS Combinatorial Science Supported p-Toluenesulfonic Acid as a Highly Robust and Eco-Friendly Isocyanide Scavenger | ACS Combinatorial Science](https://pubs.acs.org/cms/10.1021/co100035z/asset/images/medium/co-2010-00035z_0002.gif)
Supported p-Toluenesulfonic Acid as a Highly Robust and Eco-Friendly Isocyanide Scavenger | ACS Combinatorial Science
![Write the detailed mechanism for the following reaction. Give all elementary steps. (TsOH = p-Toluenesulfonic acid) | Homework.Study.com Write the detailed mechanism for the following reaction. Give all elementary steps. (TsOH = p-Toluenesulfonic acid) | Homework.Study.com](https://homework.study.com/cimages/multimages/16/index1452107932155204436.png)