p-Toluenesulfonic acid - Wikipedia
Acetone p-toluenesulfonic acid | C10H14O4S - PubChem
How did p-toluenesulfonic acid do *that*? I thought the acid would just protonate OH : r/chemhelp
organic chemistry - Verify my expected product of two acid/base reactions and does chosen solvent change reaction? - Chemistry Stack Exchange
Solved Can p-Toluenesulfonic acid be used in replacement of | Chegg.com
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 monohydrate, 97%, Thermo Scientific Chemicals
WO1990005717A1 - Preparation of 2-chloro-4-toluenesulfonic acid - Google Patents
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 -
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
p-Toluenesulfonic Acid 6192-52-5 | TCI AMERICA
Illustrated Glossary of Organic Chemistry - Toluenesulfonic acid (p-toluenesulfonic acid; TsOH; p-TsOH)
A Combination System of p-Toluenesulfonic Acid and Acetic Acid for the Hydration of Alkynes
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‐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 -
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 catalysed fluorination of α-branched ketones for the construction of fluorinated quaternary carbon centres - Chemical Communications (RSC Publishing)
![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
p-Toluenesulfonic acid | C7H7SO3H | CID 6101 - PubChem
p-Toluenesulfonic acid | CAS 104-15-4 | SCBT - Santa Cruz Biotechnology
Supported p-Toluenesulfonic Acid as a Highly Robust and Eco-Friendly Isocyanide Scavenger | ACS Combinatorial Science
Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives | SpringerLink
P-Toluenesulfonic acid - YouTube
Synthesis of TZC01. i, triethylamine, p-toluenesulfonic acid... | Download Scientific Diagram
