Zobrazeno 1 - 10
of 244
pro vyhledávání: '"E. Yu. Schmidt"'
Publikováno v:
Russian Journal of Organic Chemistry. 59:540-544
Autor:
Trofimov, B. A., Schmidt, E. Yu.
Publikováno v:
Russian Chemical Bulletin; Jul2024, Vol. 73 Issue 7, p1866-1883, 18p
Autor:
P. A. Volkov, K. O. Khrapova, I. A. Bidusenko, A. A. Telezhkin, E. Yu. Schmidt, A. I. Albanov, B. A. Trofimov
Publikováno v:
Russian Chemical Bulletin. 71:1514-1518
Autor:
E. Yu. Schmidt, B. A. Trofimov
Publikováno v:
Doklady Chemistry. 505:127-145
Publikováno v:
Russian Journal of Organic Chemistry. 54:1422-1424
Direct ethynylation of ketimines with alkynes in the superbasic system t-BuOK–DMSO has been accomplished for the first time using the reaction of (E)-N,1-diphenylethan-1-imine with 3-ethynylaniline as an example.
Publikováno v:
Russian Journal of Organic Chemistry. 54:659-661
2-Acetyl-4-methyl-3,4-dihydropyrans reacted with hydroxylamine in pyridine to give (E)-1-(4-methyl-3,4-dihydro-2H-pyran-2-yl)ethan-1-one oximes in up to 85% yield with high stereoselectivity.
Autor:
Vladimir B. Kobychev, Vladimir B. Orel, E. Yu. Schmidt, Nadezhda M. Vitkovskaya, Boris A. Trofimov
Publikováno v:
Russian Chemical Bulletin. 64:518-524
Mechanisms of ethynylation and vinylation of ketones with phenylacetylene in the presence of KOH•5DMSO superbase were studied using the MP2/6-311++G**//B3LYP/6-31+G* approach. The thermal effects and activation barriers to individual reaction stage
Publikováno v:
Russian Journal of Organic Chemistry. 52:1056-1058
Autor:
Boris A. Trofimov, E. Yu. Schmidt
Publikováno v:
Russian Chemical Reviews. 83:600-619
The main advances in the chemistry of acetylene in superbasic media achieved over the last five years are analyzed. Particular emphasis is placed on the ethynylation of aldehydes and ketones and C-, N- and O-vinylation. The cascade assembly of comple
Autor:
Shabalin, Dmitrii A.1 (AUTHOR) shabalin.chemistry@gmail.com, Zelenkov, Lev E.2,3 (AUTHOR) lev.zelenkov@metalab.ifmo.ru
Publikováno v:
ChemistrySelect. 6/13/2023, Vol. 8 Issue 22, p1-7. 7p.