p-Toluenesulfonic acid - Wikipedia
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 -
A Combination System of p-Toluenesulfonic Acid and Acetic Acid for the Hydration of Alkynes
THP Deprotection Mechanism - p-Toluenesulfonic Acid (p-TsOH)
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
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
Supported p-Toluenesulfonic Acid as a Highly Robust and Eco-Friendly Isocyanide Scavenger | ACS Combinatorial Science
p-Toluenesulfonic acid monohydrate, 97%, Thermo Scientific Chemicals
Make p-Toluenesulfonic Acid - YouTube
![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")
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
Solved Can p-Toluenesulfonic acid be used in replacement of | Chegg.com
![Para toluenesulfonic acid-catalyzed one-pot, three-component synthesis of benzo[5,6]chromeno[3,2-c]quinoline compounds in aqueous medium](https://www.degruyter.com/document/doi/10.1515/hc-2020-0128/asset/graphic/j_hc-2020-0128_ga_001.jpg "Para toluenesulfonic acid-catalyzed one-pot, three-component synthesis of benzo[5,6]chromeno[3,2-c]quinoline compounds in aqueous medium")
Para toluenesulfonic acid-catalyzed one-pot, three-component synthesis of benzo[5,6]chromeno[3,2-c]quinoline compounds in aqueous medium
organic chemistry - Verify my expected product of two acid/base reactions and does chosen solvent change reaction? - Chemistry Stack Exchange
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)
Schematic of the reaction between p-toluenesulfonic acid monohydrate... | Download Scientific Diagram
In focus: p-Toluenesulfonic acid (PTSA) – ExSyn
p‐Toluenesulfonic Acid Promoted Annulation of 2‐Alkynylanilines with Activated Ketones: Efficient Synthesis of 4‐Alkyl‐2,3‐Disubstituted Quinolines - Peng - 2010 - European Journal of Organic Chemistry - Wiley Online Library
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 - YouTube
