Zobrazeno 1 - 8
of 8
pro vyhledávání: '"S. Yu. Vyazmin"'
Autor:
Oleg B. Chakchir, Nickolay A. Knyazev, V. M. Boitsov, S. Yu. Vyazmin, Alexander V. Stepakov, Dmitrii M. Nikolaev, S. V. Shmakov
Publikováno v:
Asian Journal of Chemistry. 31:2133-2138
Benzo[h]isoquinoline scaffold is of interest as a rigid subunit that can be useful for constructing biologically active products. However, no good-yielded synthetic pathway to this ring system has been reported yet. Herein, a facile one-pot synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b811b3d4e5d376708abf540b0ed93d7a
https://doi.org/10.14233/ajchem.2019.22074
https://doi.org/10.14233/ajchem.2019.22074
Autor:
Igor E. Eliseev, Eugene N. Nikolaev, S. Yu. Vyazmin, Igor Popov, Michael V. Dubina, V. M. Boitsov, Alexey S. Kononikhin, Yu. V. Natochin
Publikováno v:
Paleontological Journal. 48:339-344
The physicochemical conditions of the aqueous environment at the dawn of biological evolution were of key importance for abiogenic peptide synthesis. Recently, we have shown theoretical and experimental evidence for the unique role of potassium ions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8343b9a4c9760cabd74ed732aeebe8
https://doi.org/10.1134/s0031030114040054
https://doi.org/10.1134/s0031030114040054
Publikováno v:
Russian Chemical Bulletin. 61:843-846
N-Phenylamide and phenyl (thio)esters of 3-phenylpropiolic acid add benzene in the presence of CF3SO3H or AlX3 (X = Cl, Br) to give 4,4-diphenyl-3,4-dihydroquinolin-2-one, 4,4-diphenyl-3,4-dihydrocoumarin, and 4,4-diphenyl-3,4-dihydrothiocoumarin, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60087dab37648792ad5518735530ba1b
https://doi.org/10.1007/s11172-012-0117-3
https://doi.org/10.1007/s11172-012-0117-3
Publikováno v:
Russian Journal of Applied Chemistry. 78:1662-1667
Application of a logistic regression to interpretation of results is illustrated by spectrophotometric data on solid-state polymerization of symmetric and asymmetric diyne carbamates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a83a957026e7c1710621605d8cf5e31f
https://doi.org/10.1007/s11167-005-0582-7
https://doi.org/10.1007/s11167-005-0582-7
Publikováno v:
Russian Journal of Organic Chemistry. 38:775-787
Carbamates of monoacetylene and diacetylene series were synthesized and characterized. A catalytic system CuI-pyrrolidine was applied for the first time to a synthesis of symmetrical diacetylenes by oxidative dimerization of terminal acetylenes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16754ea3047d4347cd9e67c105284cf0
https://doi.org/10.1023/a:1020326818084
https://doi.org/10.1023/a:1020326818084
Autor:
Igor E. Eliseev, N. V. Sibirev, Vladimir G. Dubrovskii, Yu. V. Natochin, V. M. Boitsov, Michael V. Dubina, S. Yu. Vyazmin
Publikováno v:
The Journal of chemical physics. 138(24)
The salt-induced peptide formation is important for assessing and approaching schemes of molecular evolution. Here, we present experimental data and an exactly solvable kinetic model describing the linear polymerization of L-glutamic amino acid in wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4227595effdbe3f6c54e38f0e55a237
https://pubmed.ncbi.nlm.nih.gov/23822273
https://pubmed.ncbi.nlm.nih.gov/23822273
Publikováno v:
ChemInform. 44
N-Phenylamide and phenyl (thio)esters of 3-phenylpropiolic acid add benzene in the presence of CF3SO3H or AlX3 (X = Cl, Br) to give 4,4-diphenyl-3,4-dihydroquinolin-2-one, 4,4-diphenyl-3,4-dihydrocoumarin, and 4,4-diphenyl-3,4-dihydrothiocoumarin, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9608333142fabd18286a3dde1102da2f
https://doi.org/10.1002/chin.201324028
https://doi.org/10.1002/chin.201324028
Publikováno v:
ChemInform. 33
Carbamates of monoacetylene and diacetylene series were synthesized and characterized. A catalytic system CuI-pyrrolidine was applied for the first time to a synthesis of symmetrical diacetylenes by oxidative dimerization of terminal acetylenes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a6e6c24c2e52b7b42d5461feba7e457
https://doi.org/10.1002/chin.200251117
https://doi.org/10.1002/chin.200251117