A study on the arylation of heteroatom nucleophiles by using activated haloarenes, with or without metal catalysts, is reported. A discussion concerning the involvement of traces of metals is presented, supported by an unexpected ''ligand'' effect in the absence of added metal catalysts. We believe that the frontier between nucleophilic aromatic substitution and catalysis will likely prove to be much harder to delimit than is generally thought
We present nucleophilic aromatic substitution of unsubstituted aryl chlorides via a mechanism that i...
Part I: The elimination-addition (benzyne) mechanism postulated for nucleophilic substitutions of n...
This thesis was previously restricted to Strathclyde users only until 1st October 2022.The transitio...
A study on the arylation of heteroatom nucleophiles by using activated haloarenes, with or without m...
Halogenated heterocycles are common in pharmaceutical and natural products and there is a need to de...
L'objectif central de notre thèse de doctorat visait l'utilisation d'halogénures d'aryles en tant qu...
Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium te...
Transition metal-free couplings of haloarenes with arenes, triggered by the use of alkali metal alko...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Over recent decades transition metal-catalysed cross-coupling has been developed significantly, open...
Over recent decades transition metal-catalysed cross-coupling has been developed significantly, open...
Potassium hydride behaves uniquely and differently than sodium hydride towards aryl halides. Its rea...
Potassium hydride behaves uniquely and differently than sodium hydride towards aryl halides. Its rea...
We present nucleophilic aromatic substitution of unsubstituted aryl chlorides via a mechanism that i...
Part I: The elimination-addition (benzyne) mechanism postulated for nucleophilic substitutions of n...
This thesis was previously restricted to Strathclyde users only until 1st October 2022.The transitio...
A study on the arylation of heteroatom nucleophiles by using activated haloarenes, with or without m...
Halogenated heterocycles are common in pharmaceutical and natural products and there is a need to de...
L'objectif central de notre thèse de doctorat visait l'utilisation d'halogénures d'aryles en tant qu...
Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium te...
Transition metal-free couplings of haloarenes with arenes, triggered by the use of alkali metal alko...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Recent developments in experimental and computational chemistry have identified a rapidly growing cl...
Over recent decades transition metal-catalysed cross-coupling has been developed significantly, open...
Over recent decades transition metal-catalysed cross-coupling has been developed significantly, open...
Potassium hydride behaves uniquely and differently than sodium hydride towards aryl halides. Its rea...
Potassium hydride behaves uniquely and differently than sodium hydride towards aryl halides. Its rea...
We present nucleophilic aromatic substitution of unsubstituted aryl chlorides via a mechanism that i...
Part I: The elimination-addition (benzyne) mechanism postulated for nucleophilic substitutions of n...
This thesis was previously restricted to Strathclyde users only until 1st October 2022.The transitio...