Easy Access to SCF2‐Containing Molecules through a Versatile Reagent

A new fluoroalkylmethanesulfenamide reagent was developed to synthesize various molecules bearing the SCF2CO2Me group. Furthermore, the carboxyl function was successfully post‐transformed, through C–C coupling, for easy access to molecules containing the –SCF2– functionality. A fluoroalkylmethanesul...

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Published in:European journal of organic chemistry 2017-04, Vol.2017 (14), p.1911-1914
Main Authors: Ismalaj, Ermal, Glenadel, Quentin, Billard, Thierry
Format: Article
Language:English
Subjects:
Aromatic substitution
Carbonyl compounds
Chemical synthesis
Coupling (molecular)
C–C coupling
Fluorine
Group dynamics
Sulfur
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container_end_page 1914
container_issue 14
container_start_page 1911
container_title European journal of organic chemistry
container_volume 2017
creator Ismalaj, Ermal
Glenadel, Quentin
Billard, Thierry
description A new fluoroalkylmethanesulfenamide reagent was developed to synthesize various molecules bearing the SCF2CO2Me group. Furthermore, the carboxyl function was successfully post‐transformed, through C–C coupling, for easy access to molecules containing the –SCF2– functionality. A fluoroalkylmethanesulfenamide reagent was developed to synthesize various molecules bearing the SCF2CO2Me group. Furthermore, the carboxyl function is successfully post‐transformed, through C–C coupling, for easy access to molecules containing the –SCF2– functionality.
doi_str_mv 10.1002/ejoc.201700103
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source Wiley-Blackwell Read & Publish Collection
subjects Aromatic substitution
Carbonyl compounds
Chemical synthesis
Coupling (molecular)
C–C coupling
Fluorine
Group dynamics
Sulfur
title Easy Access to SCF2‐Containing Molecules through a Versatile Reagent
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