Zobrazeno 1 - 10
of 11
pro vyhledávání: '"G. A. Shirokii"'
Autor:
K. N. Zelenin, G. A. Shirokii
Publikováno v:
Russian Journal of General Chemistry. 72:244-250
1-Acetyl- and 1-benzoyl-2- and -3-phenyliminooxoindolines were synthesized. o-(Acetylamino)phenylglyoxylic acid anil was prepared from 1-acetyl-3-phenylimino-2-oxoindoline. More stable o-(acetylamino)phenylglyoxylanilide anil can be prepared not only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56ad5473a0bbef254f43570b5888fd61
https://doi.org/10.1023/a:1015477719361
https://doi.org/10.1023/a:1015477719361
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:292-296
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::851e33e547cf2cb340543b060697a4a6
https://doi.org/10.1007/bf00474095
https://doi.org/10.1007/bf00474095
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:76-80
Isatin 2-thiosemicarbazone and its derivatives with one methyl group attached to the nitrogen atoms of the side chain exist in solution primarily in the iminohydrazine tautomeric form. Further substitution of the hydrogen atoms attached to the nitrog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f729f8b7263ec38d860a88326ac9f7da
https://doi.org/10.1007/bf00473918
https://doi.org/10.1007/bf00473918
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a47b0e0ae7f135c491da1ae3e7c9dec
https://doi.org/10.1002/chin.197419341
https://doi.org/10.1002/chin.197419341
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9571c2df6b8cf68d08f3b4da79076f0
https://doi.org/10.1002/chin.197932102
https://doi.org/10.1002/chin.197932102
Autor:
A. B. Tomchin, G. A. Shirokii
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95a1adc1438e6b374d3cee69674190bd
https://doi.org/10.1002/chin.197507107
https://doi.org/10.1002/chin.197507107
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Das Thionaphthenchinon-α-anilid (I) reagiert mit Thiosemicarbazid und Semicarbazid (II) in alkoholischer Losung unter ausschlieslicher Bildung des α-Semicarbazons und α-Thiosemicarbazons (III).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab5677c8af59f7ac4b3c53c759a17fbd
https://doi.org/10.1002/chin.197152342
https://doi.org/10.1002/chin.197152342
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecb5648af4d30d9514dfe5ae5d84e9b6
https://doi.org/10.1002/chin.197231211
https://doi.org/10.1002/chin.197231211
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de079e1e0cf7d94f2bc9f2f009179f1d
https://doi.org/10.1002/chin.197117326
https://doi.org/10.1002/chin.197117326
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84007df96ede26b519b08b177eb38c29
https://doi.org/10.1002/chin.197220277
https://doi.org/10.1002/chin.197220277