1334688-33-3

Upstream product

• 32121-04-3 N-cinnamyl-4-methylbenzenesulfonamide 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 591-50-4 iodobenzene 
• 373640-90-5 N-cinnamyl-4-methyl-N-(prop-2-yn-1-yl)-benzenesulfonamide 
• 55022-46-3 4-methyl-N-prop-2-ynylbenzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 305837-95-0 4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1598431-81-2 4-methyl-N-((3-phenyloxiran-2-yl)methyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide 
• 1598431-51-6 phenyl(4-phenyl-1-tosyl-3,4-dehydropiperidin-3-yl)methanone 
• 1334688-42-4 9-phenyl-2-(p-tolylsulfonyl)-2,3,3a,4-tetrahydro-1H-benzo[f]isoindole 
• 1312606-58-8 C₂₅H₂₃NO₂S 

Relevant academic research and scientific papers

Regio- And chemoselective synthesis of nitrogen-containing heterocycles: Via the oxidative cascade cyclization of unactivated 1, n -enynes

The development of a method for performing radical initiated intramolecular cascade cyclization of 1,n-enynes provided a competent protocol for producing structurally diverse complex heterocycles. Herein, we demonstrate I2/TBHP promoted, solven

Base-Induced Cyclization of Propargyl Alkenylsulfones: A High-Yielding Synthesis of 4,5-Disubstituted 2H-Thiopyran 1,1-Dioxides

A convenient synthesis of 4,5-disubstituted 2H-thiopyran 1,1-dioxides is reported through a base induced process starting from eneyne sulfones. Except for strongly electron-withdrawing groups, the reaction tolerated a wide variety of substituents in the t

Lewis acid mediated intramolecular C-C bond formation of alkyne-epoxide leading to six-membered nitrogen and oxygen heterocycles

Intramolecular C-C bond formation of oxygen- and nitrogen-tethered alkynes and epoxide mediated by Lewis acid under ambient conditions is described. A simple procedure for the synthesis of 3,6- and 5,6-dihydropyrans and 3,4-dehydropiperidines from acyclic