Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Oleg Dmitrievich Mitkin"'
Autor:
Alexandre V. Ivachtchenko, Oleg Dmitrievich Mitkin, S. E. Tkachenko, Eugene B. Frolov, Alexandre V. Khvat
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:170-178
A schemes have been proposed for the synthesis of novel 4-substituted 2,7-dimethyl-3,4-dihydro-1H- and previously unknown 2,7-dimethyl-cis-1,2,3,3a,4,8b-hexahydropyrrolo[3,4-b]indoles. In the case of the Dimebon structural analog 2,7-dimethyl-4-[2-(6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4912178ac58e997cc03a13e75cb0df76
https://doi.org/10.1007/s10593-010-0488-z
https://doi.org/10.1007/s10593-010-0488-z
Publikováno v:
Tetrahedron. 57:1827-1831
The method of indole preparation by transformation of 3-nitropyridinium salts was successfully extended to the synthesis of indoles containing substituents Cl, PhS, CN, Ac and COOEt on the 5-position.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::824f75b93a25d63e6291238a4080d4a0
https://doi.org/10.1016/s0040-4020(00)01162-5
https://doi.org/10.1016/s0040-4020(00)01162-5
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:871-899
Advances in the synthesis of acylpyridines, pyridinecarboxylic acids, and their derivatives involving direct functionalization of the pyridine ring and substituent modification over the past 15 years are reviewed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29665af5d0c89e99ac3637f6525f22d8
https://doi.org/10.1007/bf02311322
https://doi.org/10.1007/bf02311322
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a6dac5fc3b21168df0d4d34faca843
https://doi.org/10.1002/chin.199645167
https://doi.org/10.1002/chin.199645167
Publikováno v:
ChemInform. 29
The homolytic ethoxycarbonylation of alkyl-3-nitropyridines has been accomplished for the first time by the action of ethyl pyruvate and hydrogen peroxide in the presence of ferrous sulfate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e544051caf9ea42cf58e3c101880c9f6
https://doi.org/10.1002/chin.199820172
https://doi.org/10.1002/chin.199820172
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f172ca9ca944949bdf6b412d72cffa5
https://doi.org/10.1002/chin.200008284
https://doi.org/10.1002/chin.200008284
Publikováno v:
ChemInform. 31
Methyl triflate is an efficient agent for the quaternization of nitropyridines containing an additional electron-withdrawing substituent. When triethyloxonium hexachloroantimonate is used as the quaternizing agent, β-elimination occurs with formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30af644c714ccc39ca86675d79c22653
https://doi.org/10.1002/chin.200043155
https://doi.org/10.1002/chin.200043155
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:47-48
Methyl triflate is an efficient agent for the quaternization of nitropyridines containing an additional electron-withdrawing substituent. When triethyloxonium hexachloroantimonate is used as the quaternizing agent, β-elimination occurs with formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::253233495ee4d5a4ab3c869a02991961
https://doi.org/10.1007/bf02256843
https://doi.org/10.1007/bf02256843
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:1299-1300
The homolytic ethoxycarbonylation of alkyl-3-nitropyridines has been accomplished for the first time by the action of ethyl pyruvate and hydrogen peroxide in the presence of ferrous sulfate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dadf307c82e9bb47d78ac5afaa68e0c4
https://doi.org/10.1007/bf02320331
https://doi.org/10.1007/bf02320331
Publikováno v:
Scopus-Elsevier
Under the influence of bases, the 4-6-dimethyl-5-nitro-2-chloro-3-cyanopyridine molecule was found to undergo autohetarylation with the formation of a doubled molecule. Based on RSA data, it was found that such a process takes place exclusively at th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59aa7a4d6567d160bc49bc887a746249
http://www.scopus.com/inward/record.url?eid=2-s2.0-19844369483&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-19844369483&partnerID=MN8TOARS
