82754-33-4

Upstream product

• 105304-70-9 3-phenyl 3-fluoro 2-propenoic acid 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 4891-38-7 phenylpropynoic acid methyl ester 
• 82754-24-3 β-Fluorocinnamoyl chloride 

Relevant academic research and scientific papers

Stereoselective synthesis of (Z)-β-fluoro-α, β -unsaturated esters from (Z)-2-fluoro-1-alkenyliodonium salts

(Z)-β-Fluoro-α,β-unsaturated esters were stereoselectively synthesized from (Z)-2-fluoro-1-alkenyliodonium salts by the Pd-catalyzed methoxycarbonylation reaction. The reaction proceeded at room temperature and various functional groups on the substrate c

Mono-hydrofluorination of Electrophilic Alkynes by the Liquid Bishasic CsF-H2O-DMF System (DMF = N,N-dimethylformamide)

CsF induces the addition of HF in fair yields to activated acetylenic triple bonds in a DMF-water bishasic medium (DMF = N,N-dimethylformamide); in a homogeneous DMF-water mixture, no addition is observed.

Tetrabutylammonium and polymer-supported dihydrogentrifluoride: new reagents for the hydrofluorination of activated acetylenic bonds

Tetrabutylammonium and polymer-supported dihydrogentrifluoride are easily prepared by a phase-transfer procedure from the corresponding fluoride salts.These stable new dihydrogentrifluoride salts allow the addition of HF under mild conditions to carbon-ca

Tetrabutylammonium and Polymer-supported Dihydrogentrifluoride: New Hydrofluorinating Reagents for Electrophilic Alkynes

Tetrabutylammonium and polymer-supported dihydrogentrifluoride are readily accessible reagents which allow addition of HF to activated carbon-carbon triple bonds, thus leading to functional fluoroalkenes in good yields.