Zobrazeno 1 - 10
of 245
pro vyhledávání: '"G. Saint-Ruf"'
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 93:251-252
10-chloro-2,3,7,8-tetramethyl-, 10-chloro-2,4,6,8-tetramethyl- and 10-chloro-3,4,6,7-tetramethylphenoxarsines were prepared; the chemical shifts of the protons of these new compounds and those of 10-chlorophenoxarsine in N.M.R. spectra are reported,
Publikováno v:
Journal of Heterocyclic Chemistry. 17:81-86
The electron impact mass spectrometric fragmentation pathways for some 3-substituted derivatives of coumarin, benzo[f]coumarin, thieno[3,2-f]coumarin, thieno[2,3-h]coumarin and azacoumarin, viz nitriles, carboxamides, thiocarboxamides and esters were
Publikováno v:
Nucleic Acids Research. 15:5629-5642
The reactivity of nucleic acids in various conformations and two isosteric chemical carcinogens 2-N,N-acetoxyacetylaminofluorene (N-AcO-AAF) and 3-N,N-acetoxyacetylamino-4,6-dimethyldipyrido [1,2-a:3',2'-d] imidazole (N-AcO-AGlu-P-3) have been studie
Publikováno v:
Journal of Heterocyclic Chemistry. 23:425-431
Six dipyrido[1,2-a:3′,2′d]imidazole derivatives related to glutamic acid pyrolysates have been studied by mass spectrometry. The data indicate that there are certain ions which are characteristic of the fragmentation of this family of compounds u
Publikováno v:
Mutation Research/Environmental Mutagenesis and Related Subjects. 203:95-101
Rats were pretreated with a single oral dose of different mutagenic fractions obtained from glutamic acid pyrolysate: Glu-P-2 (2-amino-dipyrido[1,2-a:3',2'-d]imidazole), Glu-P-3 (3-amino-4,6-dimethyldipyrido[1,2-a:3',2'-d]imidazole), the tar residue
Autor:
G. Saint-Ruf, Th. Silou
Publikováno v:
Journal of Heterocyclic Chemistry. 16:1535-1539
The mass spectra of some 7-methyl, 7-chloro and 6-earbethoxythiazolo[3,2-a]pyrimidin-5-ones were studied (2,3,4). The electron impact fragmentation patterns of these compounds showed their relatively high stability and their similar mode of decomposi
Publikováno v:
Chromatographia. 11:141-144
Bentone-34, a selective adsorbent, has been studied for use in high-performance liquid chromatography (HPLC) to separate isomeric phenoxathiin derivatives. We have compared the performance of this adsorbent in gas chromatography and liquid chromatogr
Autor:
G. Saint-Ruf, J.-P. Coïc
Publikováno v:
Journal of Heterocyclic Chemistry. 15:769-772
The diacetylation of phenoxathiin under the typical conditions for Friedel-Crafts reaction results in a mixture consisting of 2,7-diacetylphcnoxathiin (3) and 2,8-diacetylphenoxathiin (9). The compound hitherto descrihed in the literature as 9 proved
Publikováno v:
Nucleic Acids Research. 12:8553-8566
The conformation of synthetic or natural DNAs modified in vitro by covalent binding of N-AcO-A-Glu-P-3 was investigated by fluorescence and circular dichroism. In all cases, substitution occurs mainly on the C8 of guanine residues. In modified poly(d
Autor:
J. P. Coic, G. Saint-Ruf
Publikováno v:
Journal of Heterocyclic Chemistry. 15:1367-1371
2-Aminophenoxathiin undergoes easy condensation with different ω-bromoketones to give 2-aroylmethylaminophenoxathiins. These compounds give pyrrolo[2,3-b]phenoxathiins by the Mohlau-Bischler cyclisation. Some carbazolo[2,1-b]phenoxathiins were also