Zobrazeno 1 - 10
of 42
pro vyhledávání: '"G. B. Erusalimskii"'
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4e9d5fd15e02524eddf8e7eb4481e7a
https://doi.org/10.1002/chin.199401123
https://doi.org/10.1002/chin.199401123
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:1027-1030
5-Substituted tetrazoles are formed by the reaction of nitriles with mono-, di-, and trialkylammonium azides in aprotic dipolar solvents and alcohols. Tetraalkylammonium azides do not react with nitriles. The formation of 5-substituted tetrazoles occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1a9c34c80101feff775385286955b35
https://doi.org/10.1007/bf00531480
https://doi.org/10.1007/bf00531480
Autor:
Buchner, Magnus R.1 (AUTHOR) magnus.buchner@chemie.uni-marburg.de, Dankert, Fabian1,2 (AUTHOR), Berthold, Chantsalmaa1 (AUTHOR), Müller, Matthias1 (AUTHOR), von Hänisch, Carsten1 (AUTHOR)
Publikováno v:
Chemistry - A European Journal. 11/24/2023, Vol. 29 Issue 66, p1-5. 5p.
Autor:
M. V. Chekushina, G. B. Erusalimskii, G. I. Koldobskii, I. Yu. Shirobokov, Vladimir A. Ostrovskii
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:413-417
Alkylation of 1-methyl-5-aryltetrazoles with dimethyl sulfate leads to the formation of 1,4-dimethyl-5-aryltetrazolium ion salts. Alkylation of isomeric 2-methyl-5-aryltetrazoles also apparently takes place at the N(4) atom. 1-Methyl-5-aryltetrazoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fafd92addbcc559225d189504e57f699
https://doi.org/10.1007/bf00478861
https://doi.org/10.1007/bf00478861
Publikováno v:
Journal of Structural Chemistry. 18:243-246
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36161a230234a05d4bf1afc089e4eb65
https://doi.org/10.1007/bf00753969
https://doi.org/10.1007/bf00753969
Publikováno v:
Macromolecules. 9:217-221
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6dc42d87ccaa1711ffdbed9423f74c5
https://doi.org/10.1021/ma60050a007
https://doi.org/10.1021/ma60050a007
Autor:
V. D. Nikolaev, V. S. Poplavskii, G. I. Koldobskii, I. E. Titova, G. B. Erusalimskii, Vladimir A. Ostrovskii
Publikováno v:
Chemistry of Heterocyclic Compounds. 22:880-883
The reaction of benzonitrile with the ammonium, alkyl-, dialkyl-, and trialkylammonium salts of hydrazoic acid in DMF at 100‡C produces 5-phenyltetrazole. The yield of 5-phenyltetrazole is practically independent of the structure of the ammonium ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5c00610972dcf82b22e718e03285726
https://doi.org/10.1007/bf01175064
https://doi.org/10.1007/bf01175064
Publikováno v:
Journal of Structural Chemistry. 14:546-548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6f57d7cceaf69e8dfa4cf944a38e061
https://doi.org/10.1007/bf00747027
https://doi.org/10.1007/bf00747027
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e594429346e8c72acd4098ca480025
https://doi.org/10.1002/chin.198730188
https://doi.org/10.1002/chin.198730188
Autor:
I. Yu. Shirobokov, G. B. Erusalimskii, G. I. Koldobskii, Vladimir A. Ostrovskii, M. V. Chekushina
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8f62eea15a08cab15bd9a8b68d3078a
https://doi.org/10.1002/chin.198843204
https://doi.org/10.1002/chin.198843204