Zobrazeno 1 - 9
of 9
pro vyhledávání: '"B. T. Oloi"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:66-70
The molecular ions of isatin (I) and N-methyl- (II) and N-ethylisatin (III) β-thiosemicarbazones undergo fragmentation via many pathways with the elimination of NH3, H2S, CO, CH2N2, CHN3, CH2N2S, CH2NS, and CHNS particles; this is due to primary loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234884a0b5c39ea4bbdee6adc52caf52
https://doi.org/10.1007/bf00471202
https://doi.org/10.1007/bf00471202
Autor:
G. I. Zhungietu, Kh. Sh. Khariton, M. A. Rekhter, N. I. Chmykhova, B. T. Oloi, N. P. Dormidontova
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:515-518
The mass spectra of N-propyl- (I), N-allyl- (IV), and N-propargylisatin (VII) and their 5-methyl (II, V, VIII) and 7-methyl (III, VI, and IX) derivatives were recorded. It is shown that a portion of the [M-2CO]+ ions in the mass spectra of N-propargy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1801e756255fc755ade0b3c85c2ce6c1
https://doi.org/10.1007/bf00473197
https://doi.org/10.1007/bf00473197
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:840-843
It is shown that in the mass spectra of N-alkylisatins with a normal C1-C10 chain the intensity of the [M-CO]+- and [M-(2CO)]+. peaks characteristic for isatin and N-methylisatin decreases as the alkyl radical is lengthened, whereas the intensity of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57fba046c628c982252441b26bdb63c6
https://doi.org/10.1007/bf00497309
https://doi.org/10.1007/bf00497309
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7dc0313afa4af62addf776af4363720
https://doi.org/10.1002/chin.197545248
https://doi.org/10.1002/chin.197545248
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::208f2d61f4c00e0cbb6e3fb1e45a0fd9
https://doi.org/10.1002/chin.197921063
https://doi.org/10.1002/chin.197921063
Autor:
N. P. Dormidontova, M. A. Rekhter, N. I. Chmykhova, B. T. Oloi, G. I. Zhungietu, Kh. Sh. Khariton
Publikováno v:
Chemischer Informationsdienst. 8
The mass spectra of N-propyl- (I), N-allyl- (IV), and N-propargylisatin (VII) and their 5-methyl (II, V, VIII) and 7-methyl (III, VI, and IX) derivatives were recorded. It is shown that a portion of the [M-2CO]+ ions in the mass spectra of N-propargy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ed084949901a3435c9b735dda447916
https://doi.org/10.1002/chin.197737184
https://doi.org/10.1002/chin.197737184
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::680f59e9c4e365662fe6f0fa76e52921
https://doi.org/10.1002/chin.197114062
https://doi.org/10.1002/chin.197114062
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35c84b6326ce130185f62942adb9201
https://doi.org/10.1002/chin.197123062
https://doi.org/10.1002/chin.197123062
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3e2463f2d8fa117aae9616f6d203a84
https://doi.org/10.1002/chin.197152060
https://doi.org/10.1002/chin.197152060