16191-87-0

Upstream product

• 16191-81-4 1-(2-chloroethylsulfonyl)-4-methoxybenzene 
• 16411-17-9 (4-methoxyphenyl)(vinyl)sulfane 
• 5535-48-8 PVS 
• 557780-43-5 4-methoxy-N-morpholinobenzenesulfonamide 
• 106-93-4 ethylene dibromide 
• 20761-70-0 1-(2-chloro-ethylsulfanyl)-4-methoxy-benzene 
• 35848-00-1 1-[(4-methoxyphenyl)-sulfonyl]ethan-2-ol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 128176-22-7 C₁₈H₂₀O₆S₂ 
• 62021-92-5 1-(2-tert-Butylperoxy-ethanesulfonyl)-4-methoxy-benzene 
• 62021-93-6 1-Methoxy-4-[2-(1-methyl-1-phenyl-ethylperoxy)-ethanesulfonyl]-benzene 
• 62022-01-9 Bis-<2-(p-methoxyphenylsulfon)-aethyl>-peroxid 
• 16191-93-8 N-<2-(4-Methoxy-phenylsulfonyl)-aethyl>-tert-butylamin 
• 885052-39-1 5-ethenesulfonyl-2-methoxybenzenesulfonyl chloride 
• 69967-36-8 4-[2-(4-methoxy-benzenesulfonyl)-ethyl]-morpholine 

Relevant academic research and scientific papers

A four-component reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, 1,2-dibromoethane, and hydrazines

A four-component reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, 1,2-dibromoethane, and hydrazines under metal-free conditions is described, providing a novel and efficient approach to 2-arylsulfonyl hydrazones. This transformation proceeds

Metal-free visible-light-promoted C(sp3)-H functionalization of aliphatic cyclic ethers using trace O2

Presented is a light-promoted C-C bond forming reaction yielding sulfone and phosphate derivatives at room temperature in the absence of metals or photoredox catalyst. This transformation proceeds in neat conditions through an auto-oxidation mechanism which is maintained through the leaching of trace amounts of O2 as sole green oxidant. This journal is

Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts

Diarylfluoromethylsulfonium salts, alternatives to freons or advanced fluorinated building blocks, are bench stable and easy-to-use sources of direct fluoromethylene (:CHF) transfer to alkenes. These salts enabled development of a trans-selective monofluorinated Johnson-Corey-Chaykovsky reaction with vinyl sulfones or vinyl sulfonamides to access synthetically challenging monofluorocyclopropane scaffolds. The described method offers rapid access to monofluorinated cyclopropane building blocks with further functionalization opportunities to deliver more complex synthetic targets diastereoselectively.

Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions

Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.

BISSULFONAMIDE COMPOUNDS AS AGONISTS OF GALR1, COMPOSITIONS, AND METHODS OF USE

Embodiments of the present invention provide bissulfonamide compounds that are agonists of GalR1. The present invention further provides compositions comprising bissulfonamide compounds that are agonists of GalR1, and methods of use of such compounds and compositions.