International audienceThe Pd-catalyzed directed thiocyanation reaction of arenes and heteroarenes by CÀHb ond activation was achieved. In the presence of an electrophilic SCN source, this original methodology offered an efficient tool to access ap anel of functionalized thiocyanated compounds (21 examples, up to 78 %yield). Post-functionalization reactions further demonstrated the synthetic utility of the approach by converting the SCN-containing molecules into value-added scaffolds
Nitriles are recurring motifs in bioactive molecules and versatile functional groups in synthetic ch...
International audienceHerein, we described a practical and efficient one-pot oxidative trifluorometh...
<div><p></p><p> <i>An efficient and simple method for the preparation of 1-methyl-3-(...
International audienceThe Pd-catalyzed directed thiocyanation reaction of arenes and heteroarenes by...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Palladium-catalyzed activation of carbon–sulfur bonds allows aryne insertion into aryl thiocyanates ...
International audienceThe practical and mild aerobic oxidative CuCN-mediated cyanation of thiophenol...
A direct and straightforward thiocyanation of enamides with NH4SCN under metal-free conditions has b...
Unprecedented one-pot thiocyanofunctionalizations of terminal alkynes to deliver alkynylthiocyanates...
Alkyl thiocyanates are prevalent in natural products, drugs, and biologically active compounds. We r...
International audienceA new methodology was developed to access isothiazolone derivatives from simpl...
<div><p>A green and regioselective thiocyanation of aromatic and heteroaromatic compounds has been a...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
An easily removable pyrimidine-based auxiliary has been employed for the remote meta-C-H cyanation o...
We report herein an efficient Pd-catalyzed direct C-H bond functionalization of heteroarenes via an ...
Nitriles are recurring motifs in bioactive molecules and versatile functional groups in synthetic ch...
International audienceHerein, we described a practical and efficient one-pot oxidative trifluorometh...
<div><p></p><p> <i>An efficient and simple method for the preparation of 1-methyl-3-(...
International audienceThe Pd-catalyzed directed thiocyanation reaction of arenes and heteroarenes by...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Palladium-catalyzed activation of carbon–sulfur bonds allows aryne insertion into aryl thiocyanates ...
International audienceThe practical and mild aerobic oxidative CuCN-mediated cyanation of thiophenol...
A direct and straightforward thiocyanation of enamides with NH4SCN under metal-free conditions has b...
Unprecedented one-pot thiocyanofunctionalizations of terminal alkynes to deliver alkynylthiocyanates...
Alkyl thiocyanates are prevalent in natural products, drugs, and biologically active compounds. We r...
International audienceA new methodology was developed to access isothiazolone derivatives from simpl...
<div><p>A green and regioselective thiocyanation of aromatic and heteroaromatic compounds has been a...
A palladium-catalyzed regioselective C–H cyanation of heteroarenes was achieved using <i>tert</i>-bu...
An easily removable pyrimidine-based auxiliary has been employed for the remote meta-C-H cyanation o...
We report herein an efficient Pd-catalyzed direct C-H bond functionalization of heteroarenes via an ...
Nitriles are recurring motifs in bioactive molecules and versatile functional groups in synthetic ch...
International audienceHerein, we described a practical and efficient one-pot oxidative trifluorometh...
<div><p></p><p> <i>An efficient and simple method for the preparation of 1-methyl-3-(...