An efficient and simple radical chain reaction to convert terminal alkynes into arenesulfonylmethylcyclopentanes is described. The reaction involves a radical addition-translocation-cyclization process and necessitates solely the use of readily available arenesulfonyl chlorides in tetrahydrofuran. Interestingly, this radical-mediated C-H activation process took place with a high level of retention of configuration when an enantiomerically pure starting material was used
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
An efficient and simple radical chain reaction to convert terminal alkynes into arenesulfonylmethylc...
A new strategy for the activation of aryl sulfones towards homolytic and heterolytic cleavage via in...
The synergy between metal catalysis and radical chemistry allows to surpass previous limitations of ...
A new strategy for the transformation of terminal alkynes to branched allylic sulfones was developed...
Sulfinyl radicals – one of the fundamental classes of S-centered radicals – have eluded synthetic ap...
A sulfur-mediated electrophilic cyclization reaction of aryl-tethered internal alkynes has been deve...
Sulfinyl radicals – one of the fundamental classes of S-centered radicals – have eluded synthetic ap...
Sulfonyl chlorides are inexpensive reactants extensively explored for functionalization, but never c...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
Conclusions The paper reported a simple and efficient copper-catalyzed iminyl radical-mediated C–C ...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
An efficient and simple radical chain reaction to convert terminal alkynes into arenesulfonylmethylc...
A new strategy for the activation of aryl sulfones towards homolytic and heterolytic cleavage via in...
The synergy between metal catalysis and radical chemistry allows to surpass previous limitations of ...
A new strategy for the transformation of terminal alkynes to branched allylic sulfones was developed...
Sulfinyl radicals – one of the fundamental classes of S-centered radicals – have eluded synthetic ap...
A sulfur-mediated electrophilic cyclization reaction of aryl-tethered internal alkynes has been deve...
Sulfinyl radicals – one of the fundamental classes of S-centered radicals – have eluded synthetic ap...
Sulfonyl chlorides are inexpensive reactants extensively explored for functionalization, but never c...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
Conclusions The paper reported a simple and efficient copper-catalyzed iminyl radical-mediated C–C ...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...
International audienceA straightforward and high-yielding access to various [2.2]paracyclophanes pos...