Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous acid. In a series of later publications he reported that phenols and aromatic halides are formed by the decomposition of these diazonium salts. However it was not until 1884 that Sandmeyer discovered the ability of cuprous salts to catalyze the conversion of diazonium salts to aryl chlorides and aryl bromides. Since this time this reaction, which bears his name, has been used in most of the preparative work involving the replacement of the diazonium group by these atoms. From the time of their discovery until the present time these reactions have been the object of the study of many organic chemists. The original purpose of this research pro...
Activated carbon products modified with a benzene sulfonic acid group were prepared based on the spo...
A continued study of the recently discovered diazotizative allylation (DiazAll) reaction of aniline ...
International audienceActivated carbon products modified with benzoic, benzenesulfonic and benzylpho...
Diarryl ethers have been prepared by various candidates for master\u27s and bachelor\u27s degrees at...
The use of diazonium salts for aryl radical generation and C-H arylation processes has been known si...
A brief review of the dediazoniation of benzenediazonium salts and cyclisation reactions through 2,2...
It has been reported through work in the field of diazo chemistry that normal reactions of diazo ket...
The reactions between strongly electron-rich aromatic substrates (1,3,5-tris(N,N-dialkylamino)benzen...
Arene diazonium salts are common, easily prepared and highly useful intermediates in organic synthes...
In furtherance of the study of the mechanism of the Pschorr and related reactions the decompositions...
Les sels de diazoniums sont des électrophiles particulièrement réactifs et versatiles. Leur réputati...
A clean preparation of aryl diazonium ions using methyl nitrite is described. Further reaction of th...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
Nucleophilic substitution by S_Nl -type mechanisms is familiar in aliphatic compounds but is uncommo...
Activated carbon products modified with a benzene sulfonic acid group were prepared based on the spo...
A continued study of the recently discovered diazotizative allylation (DiazAll) reaction of aniline ...
International audienceActivated carbon products modified with benzoic, benzenesulfonic and benzylpho...
Diarryl ethers have been prepared by various candidates for master\u27s and bachelor\u27s degrees at...
The use of diazonium salts for aryl radical generation and C-H arylation processes has been known si...
A brief review of the dediazoniation of benzenediazonium salts and cyclisation reactions through 2,2...
It has been reported through work in the field of diazo chemistry that normal reactions of diazo ket...
The reactions between strongly electron-rich aromatic substrates (1,3,5-tris(N,N-dialkylamino)benzen...
Arene diazonium salts are common, easily prepared and highly useful intermediates in organic synthes...
In furtherance of the study of the mechanism of the Pschorr and related reactions the decompositions...
Les sels de diazoniums sont des électrophiles particulièrement réactifs et versatiles. Leur réputati...
A clean preparation of aryl diazonium ions using methyl nitrite is described. Further reaction of th...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
Nucleophilic substitution by S_Nl -type mechanisms is familiar in aliphatic compounds but is uncommo...
Activated carbon products modified with a benzene sulfonic acid group were prepared based on the spo...
A continued study of the recently discovered diazotizative allylation (DiazAll) reaction of aniline ...
International audienceActivated carbon products modified with benzoic, benzenesulfonic and benzylpho...