p-Toluenesulfonic acid monohydrate, 99%, extra pure, Thermo Scientific Chemicals, Quantity: 5 g | Fisher Scientific
Solved What is the full electron pushing mechanism of this | Chegg.com
p-Toluenesulfonic acid doped polystyrene (PS-PTSA): solvent-free microwave assisted cross-coupling-cyclization–oxidation to build one-pot diversely functionalized pyrrole from aldehyde, amine, active methylene, and nitroalkane - ScienceDirect
Solved Consider the acid-base equilibrium reaction of PTSA | Chegg.com
p-TSA@nano SiO2 as a New and Efficient Nanocatalyst for the One-Pot Multi-component Synthesis of Some Novel 1-Amidoalkyl-2-Naphthols Under Solvent-Free Conditions | SpringerLink
PTSA.H2O‐Catalyzed Reaction of 3‐Aminocoumarins and Phenylacetaldehydes: A Route to Access Various Pyrido(2,3‐c)coumarin Derivatives - Belal - 2017 - ChemistrySelect - Wiley Online Library
Material Safety for P-Toluenesulfonic Acid - Capital Resin
One-Pot Three Component Domino Reaction for the Synthesis of Novel Isoxazolo[2,3-c][1,3,5]Thiadiazepin-2-Ones Catalyzed by PTSA—A Green Chemistry Approach
Iodoarene-Mediated α-Tosyloxylation of Ketones with MCPBA and p-Toluenesulfonic Acid
PtO 2 /PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups - RSC Advances (RSC Publishing) DOI:10.1039/C8RA00564H
Scheme 4. Synthetic utilities of this reaction. PTSA =... | Download Scientific Diagram
p-Toluenesulfonic acid - Wikipedia
PTSA-Catalyzed Reaction of Alkyl/Aryl Methyl Ketones with Aliphatic Alcohols in the Presence of Selenium Dioxide: A Protocol for the Generation of an α-Ketoacetals Library | ACS Omega
Para toluenesulfonic acid-catalyzed one-pot, three-component synthesis of benzo[5,6]chromeno[3,2-c]quinoline compounds in aqueous medium
p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions - ScienceDirect