Mercury(II) oxide-tetrafluproboric acid reacts vyith arenes under mild or very mild conditions to afford, after treatment with iodine in a 'one-stage' reaction, the corresponding aryl iodide. The orientation is that expected based on general aromatic substitution theory and hence the meta-iodinated derivatives of deactivated arenes are accessible
A modifiable or removable pyrimidyldiisopropylsilyl (PyrDipSi) directing group for double-fold symme...
Iodination of aromatic compounds was accomplished using the procedure given by Durand, with a few sl...
A transition-metal-free, mild, and highly regioselective synthesis of nitroarenes from arenes has be...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
The first one-pot synthesis of neutral and electron-rich [hydroxy(tosyloxy)iodo]arenes (HTIBs) from ...
Reaction of aromatic compounds with bis(pyridine)iodonium(I) tetrafluoroborate (IPy2BF4) in the pres...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we p...
A mild method to prepare aryl and heteroaryl iodides by sequential C–H borylation and iodination is ...
Benzene, halobenzenes, and a number of more or less deactivated arenes,including nitrobenzene, readi...
Abstract: Easy, cheap, safe and effective preparative procedures to obtain symmetrical diaryliodoniu...
The KI-DMSO in aqueous hydrochloride has been utilized for selective iodination of activated arenes....
Benzene, halobenzenes, and a number of more or less deactivated arenes,including nitrobenzene, readi...
A mild, metal-free bromination method of arenes has been developed using the combination of bis(trif...
The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found th...
A modifiable or removable pyrimidyldiisopropylsilyl (PyrDipSi) directing group for double-fold symme...
Iodination of aromatic compounds was accomplished using the procedure given by Durand, with a few sl...
A transition-metal-free, mild, and highly regioselective synthesis of nitroarenes from arenes has be...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
The first one-pot synthesis of neutral and electron-rich [hydroxy(tosyloxy)iodo]arenes (HTIBs) from ...
Reaction of aromatic compounds with bis(pyridine)iodonium(I) tetrafluoroborate (IPy2BF4) in the pres...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we p...
A mild method to prepare aryl and heteroaryl iodides by sequential C–H borylation and iodination is ...
Benzene, halobenzenes, and a number of more or less deactivated arenes,including nitrobenzene, readi...
Abstract: Easy, cheap, safe and effective preparative procedures to obtain symmetrical diaryliodoniu...
The KI-DMSO in aqueous hydrochloride has been utilized for selective iodination of activated arenes....
Benzene, halobenzenes, and a number of more or less deactivated arenes,including nitrobenzene, readi...
A mild, metal-free bromination method of arenes has been developed using the combination of bis(trif...
The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found th...
A modifiable or removable pyrimidyldiisopropylsilyl (PyrDipSi) directing group for double-fold symme...
Iodination of aromatic compounds was accomplished using the procedure given by Durand, with a few sl...
A transition-metal-free, mild, and highly regioselective synthesis of nitroarenes from arenes has be...