A new method for the synthesis of allyl aromatic compounds not involving any metal-containing reagent or catalyst has been developed. Arylamines substituted with a large number of different substituents were converted via diazotizative deamination with tert-butyl nitrite in allyl bromide and acetonitrile to the corresponding allyl aromatic compounds. The allylation reaction was found to be suitable for larger scale synthesis due to short reaction times, a nonextractive workup, and robustness toward moisture, air, and type of solvent
[[abstract]]A simple and practical approach has been developed for conducting direct, homoallylic al...
A variety of methylarenes were successfully converted into the corresponding aromatic nitriles in go...
Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous...
A continued study of the recently discovered diazotizative allylation (DiazAll) reaction of aniline ...
Organoboron compounds have been widely used in carbon-carbon bond formation reactions in organic syn...
International audienceA clean method has been developed for the α-allylation of phenyl and alpha alk...
Allylic moiety, an important structural motif in organic chemistry, can be easily transformed into m...
These reactions can be carried out directly on aromatic amines (initial in situ acetanilide formati...
The Pd-catalyzed cross-coupling reaction of aromatic iodides and bromides with allylboronic acid est...
The formation of C–N bonds with aryl amines is one of the most widely studied reactions in organic c...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A clean preparation of aryl diazonium ions using methyl nitrite is described. Further reaction of th...
The functionalization of aromatic halides or aromatic compounds bearing substituents like fluorosulf...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel approach to aryl or alkenyl nitriles from benzyl and allyl halides has been developed. A tan...
[[abstract]]A simple and practical approach has been developed for conducting direct, homoallylic al...
A variety of methylarenes were successfully converted into the corresponding aromatic nitriles in go...
Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous...
A continued study of the recently discovered diazotizative allylation (DiazAll) reaction of aniline ...
Organoboron compounds have been widely used in carbon-carbon bond formation reactions in organic syn...
International audienceA clean method has been developed for the α-allylation of phenyl and alpha alk...
Allylic moiety, an important structural motif in organic chemistry, can be easily transformed into m...
These reactions can be carried out directly on aromatic amines (initial in situ acetanilide formati...
The Pd-catalyzed cross-coupling reaction of aromatic iodides and bromides with allylboronic acid est...
The formation of C–N bonds with aryl amines is one of the most widely studied reactions in organic c...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A clean preparation of aryl diazonium ions using methyl nitrite is described. Further reaction of th...
The functionalization of aromatic halides or aromatic compounds bearing substituents like fluorosulf...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel approach to aryl or alkenyl nitriles from benzyl and allyl halides has been developed. A tan...
[[abstract]]A simple and practical approach has been developed for conducting direct, homoallylic al...
A variety of methylarenes were successfully converted into the corresponding aromatic nitriles in go...
Diazonium salts were first prepared by Griess in 1858 by the reaction of aromatic amines and nitrous...