Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Y. Mettey"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:961-964
A series of bicyclic enols 3 and tricyclic benzo[c]quinoliziniums 4 and 5 were prepared and evaluated as inhibitors of protein kinase CKII. Of the seventeen derivatives examined, 6-hydroxy-benzo[c]quinolizinium5d was the most potent inhibitor and exh
Publikováno v:
Synthetic Communications. 24:793-802
Heterocyclic imine-enamines 1 were prepared from metalated methyl substituted heterocycles and aromatic nitriles and then oxidized with lead tetracetate to give various tetraarylpyrroles 2.
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:377-380
The unit cell of the title compound, tetrakis(μ-acetato-O:O')bis{[11-aminodibenzo[b,f][1,4]thiazepine-N 10 ]rhodium(II)}(Rh-Rh), [Rh(C 2 H 3 O 2 ) 4 (C 13 H 10 N 2 S) 2 ], contains four discrete dimer molecules which have an inversion centre. The Rh
Publikováno v:
ChemInform. 22
C 14 H 9 N 3 S cristallise dans P2 1 /c avec a=7,698, b=18,436, c=8,360 A, β=107,09°, Z=4; affinement jusqu'a R=0,035. La molecule est approximativement plane. Toutes les liaisons des cycles B et C non benzeniques ont au moins un caractere π parti
Publikováno v:
ChemInform. 23
Heteroarylmethylation of halogenobenzonitriles in the presence of air (O 2 ) gives 1-hydroxy-3-oxo-1-aryl-1H,3H-isoindoles in liquid ammonia. A one-pot or two-step synthesis is described and a mechanism is proposed
Autor:
Y. Mettey, J.‐M. Vierfond
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 27
Heterocyclic imine-enamines 1 were prepared from metalated methyl substituted heterocycles and aromatic nitriles and then oxidized with lead tetracetate to give various tetraarylpyrroles 2.
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
The reaction of balogenobenzonitriles with 2-aminobenzenethiol is a new route, in a “one-pot” or two-step approach, to 11-aminodibenzo[b,f][1,4]thiazepine and fluoro derivatives.
Publikováno v:
Journal of Heterocyclic Chemistry. 34:465-467
The reaction of balogenobenzonitriles with 2-aminobenzenethiol is a new route, in a “one-pot” or two-step approach, to 11-aminodibenzo[b,f][1,4]thiazepine and fluoro derivatives.