The fragmentation of N-acyl-isoxazol-5-ones using visible light photoredox catalysis has been disclosed. The catalyst-controlled divergent mechanisms, namely the oxidative and reductive quenching catalytic cycle, are utilized. Various oxazoles and 1,3-oxazin-6-ones are selectively obtained from the same isoxazol-5-one skeleton under mild conditions
A synthetic pathway to 3‐methylisoxazolo[4,5‐d]pyridazine and some of its derivatives is described. ...
Tetrasubstituted imidazoles can be formed in a photochemical one-pot synthesis from aldehydes, α-ami...
Whereas 2H-benztriazoles are photochemically stable, 1H-benztriazoles yield biradicals after splitin...
N-acylisoxazol-5-ones are converted into the corresponding 2-substitued oxazoles by photolysis at 30...
A continuous flow process is presented, which directly converts isoxazoles into their oxazole counte...
N-Acylisoxazol-5-ones lose carbon dioxide under photochemical and thermal conditions affording imino...
4-Trideuterioacetyl-5-methyl-3-phenyl-isoxazole ([CD3CO]-27), upon irradiation with 254 nm light, wa...
The mechanisms of the three reaction pathways for the photochemical transformation of 3,5-dimethylis...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox ...
Two approaches were developed for the conversion of isoxazol-5-ones to 2,3-dihydro-6<i>H</i>-1,3-oxa...
FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPTwo approaches were developed for the c...
5-Oxodihydroisoxazoles react with thiocarbonyl chlorides to afford N-thioacylisoxazol-5(2H)-ones whi...
Photochemically induced intramolecular hydrogen atom transfer in oxazolones is reported. An acetal o...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
A synthetic pathway to 3‐methylisoxazolo[4,5‐d]pyridazine and some of its derivatives is described. ...
Tetrasubstituted imidazoles can be formed in a photochemical one-pot synthesis from aldehydes, α-ami...
Whereas 2H-benztriazoles are photochemically stable, 1H-benztriazoles yield biradicals after splitin...
N-acylisoxazol-5-ones are converted into the corresponding 2-substitued oxazoles by photolysis at 30...
A continuous flow process is presented, which directly converts isoxazoles into their oxazole counte...
N-Acylisoxazol-5-ones lose carbon dioxide under photochemical and thermal conditions affording imino...
4-Trideuterioacetyl-5-methyl-3-phenyl-isoxazole ([CD3CO]-27), upon irradiation with 254 nm light, wa...
The mechanisms of the three reaction pathways for the photochemical transformation of 3,5-dimethylis...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox ...
Two approaches were developed for the conversion of isoxazol-5-ones to 2,3-dihydro-6<i>H</i>-1,3-oxa...
FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPTwo approaches were developed for the c...
5-Oxodihydroisoxazoles react with thiocarbonyl chlorides to afford N-thioacylisoxazol-5(2H)-ones whi...
Photochemically induced intramolecular hydrogen atom transfer in oxazolones is reported. An acetal o...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
A synthetic pathway to 3‐methylisoxazolo[4,5‐d]pyridazine and some of its derivatives is described. ...
Tetrasubstituted imidazoles can be formed in a photochemical one-pot synthesis from aldehydes, α-ami...
Whereas 2H-benztriazoles are photochemically stable, 1H-benztriazoles yield biradicals after splitin...