Zobrazeno 1 - 7
of 7
pro vyhledávání: '"A. E. Vartanova"'
Autor:
A. E. Vartanova, A. Yu. Plodukhin, M. A. Boichenko, V. V. Shorokhov, S. S. Zhokhov, I. V. Trushkov, O. A. Ivanova
Publikováno v:
Russian Chemical Bulletin. 71:2431-2440
Autor:
Anna E. Vartanova, Andrey Yu Plodukhin, Victor B. Rybakov, Mikhail N Anisimov, Nina K. Ratmanova, Olga A. Ivanova, Ivan A. Andreev, Igor V. Alabugin, Nikita Gudimchuk, Igor V. Trushkov, Irina I. Levina
Publikováno v:
Journal of the American Chemical Society. 143:13952-13961
The importance of intramolecular constraints in cyclic transition-state geometries is especially pronounced in n-endo-tet cyclizations, where the usual backside approach of a nucleophile to the breaking bond is impossible for the rings containing les
Publikováno v:
The Journal of Organic Chemistry. 86:12300-12308
A scandium trifluoromethanesulfonate-catalyzed reaction of donor-acceptor cyclopropanes with 6-amino-1,3-dimethyluracil was found to proceed as three-membered ring opening via nucleophilic attack of the C(5) atom of an ambident nucleophile serving as
Autor:
Anna E. Vartanova, Irina I. Levina, Nina K. Ratmanova, Ivan A. Andreev, Olga A. Ivanova, Igor V. Trushkov
Publikováno v:
Organicbiomolecular chemistry. 20(39)
Lewis acid-catalysed reactions of donor-acceptor cyclopropanes with 1,3-disubstituted 5-aminopyrazoles were investigated. Under catalysis with gallium(III) chloride, products of the three-membered ring opening
Autor:
Anna E, Vartanova, Andrey Yu, Plodukhin, Nina K, Ratmanova, Ivan A, Andreev, Mikhail N, Anisimov, Nikita B, Gudimchuk, Victor B, Rybakov, Irina I, Levina, Olga A, Ivanova, Igor V, Trushkov, Igor V, Alabugin
Publikováno v:
Journal of the American Chemical Society. 143(34)
The importance of intramolecular constraints in cyclic transition-state geometries is especially pronounced in
Autor:
Alexander A. Titov, Alexey V. Varlamov, Tatiana N. Borisova, Leonid G. Voskressensky, Alexander V. Aksenov, Maria D. Matveeva, A. E. Vartanova, Victor N. Khrustalev
Publikováno v:
RSC Advances. 6:74068-74071
A route towards pyrrolo[2,1-a]isoquinolines through a 3CR of 1-aroyl dihydroisoquinolines, activated alkynes and alcohols has been developed.
Autor:
Alexander A. Titov, Victor N. Khrustalev, A. E. Vartanova, Alexey V. Varlamov, Maria D. Matveeva, Alexander V. Aksenov, Tatiana N. Borisova, Leonid G. Voskressensky
Publikováno v:
ChemInform. 47
A route towards pyrrolo[2,1-a]isoquinolines through a 3CR of 1-aroyl dihydroisoquinolines, activated alkynes and alcohols has been developed.