Zobrazeno 1 - 10
of 10
pro vyhledávání: '"G. G. Krasovskaya"'
Publikováno v:
Russian Journal of Organic Chemistry. 53:1085-1089
A procedure has been developed for the synthesis of (5-alkenyl-1,2,4-oxadiazol-3-yl)anilines by selective reduction of the nitro group in 5-alkenyl-3-(nitrophenyl)-1,2,4-oxadiazoles. The resulting amines are promising monomers for oxidative and radic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32032901deb10728a82a2d811c3cebee
https://doi.org/10.1134/s1070428017070211
https://doi.org/10.1134/s1070428017070211
Publikováno v:
Russian Chemical Bulletin. 66:867-869
A synthesis new aryl alicyclic tricarboxylic acids bearing two carboxyl groups at either cyclohexane or norbornane fragment and one carboxyl group at the benzene ring was devel-oped. Tricarboxylic acids of this type are promising monomers for the syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6acd454d063d90b2e4a0f28fd8ef2355
https://doi.org/10.1007/s11172-017-1820-x
https://doi.org/10.1007/s11172-017-1820-x
Publikováno v:
Russian Journal of Organic Chemistry. 51:982-987
Two procedures have been proposed for the synthesis of pure (E)- and (Z)-3-(5-aryl-1,3,4-oxadiazol-2-yl)acrylic acids, by one-step cyclization of (Z)-4-(2-aroylhydrazinyl)-4-oxobut-2-enoic acids or via initial cyclization of (Z)-4-(2-aroylhydrazinyl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abc9b84b58e79a188e741ad3549390c9
https://doi.org/10.1134/s1070428015070155
https://doi.org/10.1134/s1070428015070155
Publikováno v:
Russian Journal of Organic Chemistry. 47:1874-1877
The formation of N′-(benzoyloxy)benzenecarboximidamides and their subsequent cyclization to 3,5-disubstituted 1,2,4-oxadiazoles in different solvents were studied. A probable reaction mechanism was proposed on the basis of the obtained results.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3f52cce4e4b0472a9d84774e76f3146
https://doi.org/10.1134/s1070428011120153
https://doi.org/10.1134/s1070428011120153
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5246367146bec90172b0137d76870696
https://doi.org/10.1002/chin.199439198
https://doi.org/10.1002/chin.199439198
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beb3b4a7fe26fdda90c62e932f46d86f
https://doi.org/10.1002/chin.199545110
https://doi.org/10.1002/chin.199545110
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac2d5922e502c8a2910c7ec3dd302bb4
https://doi.org/10.1002/chin.200018039
https://doi.org/10.1002/chin.200018039
Publikováno v:
ChemInform. 31
The corresponding heterylphthalonitriles are obtained in the reaction of 4-nitrophthalonitrile with heterocyclic N-nucleophiles in the presence of potassium carbonate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2e88e8a37cdc2c842b6aec317d643de
https://doi.org/10.1002/chin.200035027
https://doi.org/10.1002/chin.200035027
Publikováno v:
Chemistry of Heterocyclic Compounds. 35:1342-1344
The corresponding heterylphthalonitriles are obtained in the reaction of 4-nitrophthalonitrile with heterocyclic N-nucleophiles in the presence of potassium carbonate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5a933d5718633572bcf8cb7d51b8327
https://doi.org/10.1007/bf02252006
https://doi.org/10.1007/bf02252006
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71e95d8856cd0a700adca1f42cb75759
https://doi.org/10.1002/chin.198951065
https://doi.org/10.1002/chin.198951065