Nucleophilic substitution by S_Nl -type mechanisms is familiar in aliphatic compounds but is uncommon with aromatic compounds because of the general difficulty of generating vinyl cations. There is only one class of aromatic compounds for which an S_Nl-mechanism has been well established, namely diazonium salts. The evidence is persuasive that diazonium salts decompose in aqueous solution to form first an aryl cation which subsequently reacts rapidly with available nucleophiles (e.g. water or halide ions) to form the reaction products
We investigate the mechanism of SNAr fluorination reactions under the influence of protic solvents a...
The rates of aromatic nucleophilic substitution reactions in liquid ammonia are much faster than tho...
This thesis concerns the preparation and use of diaryliodonium salts. In Project I various unsymmetr...
The products of hydrolysis of some unsymmetrically substituted diphenyliodonium salts to phenols and...
Aromatic diazonium salts belong to an important class of organic compounds. The chemistry of these c...
AbstractAromatic diazonium salts belong to an important class of organic compounds. The chemistry of...
Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous...
The reactions between strongly electron-rich aromatic substrates (1,3,5-tris(N,N-dialkylamino)benzen...
Organic chemists have the ability to create complex organic molecules by connecting molecular buildi...
Benzenoid rings are prevalent in pharmaceutical drug molecules, agrochemical molecules and even in s...
Substituted benzenoid rings are a prevalent motif in many industries including high tech, agrochemic...
The reactions of aromatic and aliphatic acyl halides with hydroxylic molecules under solvolytic cond...
We report novel insights into the cascade rearrangement of destabilized vinyl cations deriving from ...
Diarryl ethers have been prepared by various candidates for master\u27s and bachelor\u27s degrees at...
In this review, we give a concise but complete overview of methods describing the use of aryl diazon...
We investigate the mechanism of SNAr fluorination reactions under the influence of protic solvents a...
The rates of aromatic nucleophilic substitution reactions in liquid ammonia are much faster than tho...
This thesis concerns the preparation and use of diaryliodonium salts. In Project I various unsymmetr...
The products of hydrolysis of some unsymmetrically substituted diphenyliodonium salts to phenols and...
Aromatic diazonium salts belong to an important class of organic compounds. The chemistry of these c...
AbstractAromatic diazonium salts belong to an important class of organic compounds. The chemistry of...
Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous...
The reactions between strongly electron-rich aromatic substrates (1,3,5-tris(N,N-dialkylamino)benzen...
Organic chemists have the ability to create complex organic molecules by connecting molecular buildi...
Benzenoid rings are prevalent in pharmaceutical drug molecules, agrochemical molecules and even in s...
Substituted benzenoid rings are a prevalent motif in many industries including high tech, agrochemic...
The reactions of aromatic and aliphatic acyl halides with hydroxylic molecules under solvolytic cond...
We report novel insights into the cascade rearrangement of destabilized vinyl cations deriving from ...
Diarryl ethers have been prepared by various candidates for master\u27s and bachelor\u27s degrees at...
In this review, we give a concise but complete overview of methods describing the use of aryl diazon...
We investigate the mechanism of SNAr fluorination reactions under the influence of protic solvents a...
The rates of aromatic nucleophilic substitution reactions in liquid ammonia are much faster than tho...
This thesis concerns the preparation and use of diaryliodonium salts. In Project I various unsymmetr...