Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Dar'ya V. Spiridonova"'
Autor:
Andrey V. Khramchikhin, Mariya A. Skryl’nikova, Maxim A. Gureev, Vladimir V. Zarubaev, Iana L. Esaulkova, Polina A. Ilyina, Oussama Abdelhamid Mammeri, Dar’ya V. Spiridonova, Yuri B. Porozov, Vladimir A. Ostrovskii
Publikováno v:
Molecules, Vol 28, Iss 21, p 7427 (2023)
A novel method for synthesizing 1,2,4-triazole- and tetrazole-containing 4H-thiopyrano[2,3-b]quinolines using a new combination of the thio-Michael and aza-Morita–Baylis–Hillman reactions was developed. Target compounds were evaluated for their c
Externí odkaz:
https://doaj.org/article/9eaf67032beb471589bde340bd8a037b
Autor:
Ivan P. Mosiagin, Olesya A. Tomashenko, Dar’ya V. Spiridonova, Mikhail S. Novikov, Sergey P. Tunik, Alexander F. Khlebnikov
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1490-1498 (2021)
A wide range of derivatives with new pyrido[2,1-a]pyrrolo[3,4-c]isoquinoline skeleton was synthesized by free-radical intramolecular cyclization of o-bromophenyl-substituted pyrrolylpyridinium salts using the (TMS)3SiH/AIBN system. The cyclization pr
Externí odkaz:
https://doaj.org/article/ea7c63f1ec934598895b49389322e61a
Publikováno v:
Inorganics, Vol 9, Iss 9, p 69 (2021)
The reaction in the system CuII/sacNa(H)/NCNR2 (sacNa(H) = sodium saccharinate (saccharin); R = Me, Et) results in the formation of the complexes [Cu(sac)2(NCNR2)(H2O)2] (R = Me 1, Et 2) instead of the expected products derived from the saccharin–c
Externí odkaz:
https://doaj.org/article/a272930eb7794122b4d2cbd3eaefb07b
Autor:
Yulia V. Krivolapova, Olesya A. Tomashenko, Liya D. Funt, Dar'ya V. Spiridonova, Mikhail S. Novikov, Alexander F. Khlebnikov
Publikováno v:
Organic & Biomolecular Chemistry. 20:5434-5443
Selective synthesis of azirine-triazole hybrids and their use in preparation of pyrrole-triazole and pyrrole-triazole-pyridine hybrids are reported.
Autor:
Yulia A. Trukhanova, Inna I. Terninko, Dar'ya V. Spiridonova, Yulia E. Generalova, Roman Ermachenkov, Galina M. Alekseeva, Elena V. Kuvaeva, Igor P. Yakovlev
Publikováno v:
ChemistrySelect. 8
Autor:
Ekaterina A. Filatova, Dmitrii Y. Smolyak, Semyon V. Tsybulin, Valery A. Ozeryanskii, Anna V. Gulevskaya, Alexander F. Pozharskii, Dar’ya V. Spiridonova
Publikováno v:
Crystal Growth & Design. 21:7247-7256
Continuing the studies of proton sponge-based oligo(arylene-ethynylenes), the protonation of the para-ortho-para-linked trimer (POP-trimer) has been investigated. For the first time, selective mono...
Autor:
Dar’ya V. Spiridonova, Irina A. Boyarskaya, Alexander Yu. Ivanov, Aleksander V. Vasilyev, Marina А. Borisova, Dmitry S. Ryabukhin, Mikhail O. Kompanets
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:1007-1016
N,O-Diprotonated forms (dications) of various quinolinecarbaldehydes were theoretically studied by DFT calculations. It was found that the most reactive electrophilic dications are expected to be generated from 2- and 4-quinolinecarbaldehydes compare
Autor:
Marie Colmont, Olivier Mentré, Diana O. Nekrasova, Dmitry O. Charkin, Oleg I. Siidra, Artem S. Borisov, Anatoly N. Zaitsev, Dar’ya V. Spiridonova
Publikováno v:
Mineralogical Magazine. 85:831-845
We report the crystal structures of eight new synthetic multinary Rb–Cu sulfates representing four new structure types: δ-Rb2Cu(SO4)2, γ-RbNaCu(SO4)2, γ-RbKCu(SO4)2, Rb2Cu2(SO4)3, Rb2Cu2(SO4)3(H2O), β-Rb2Cu(SO4)Cl2, β-Rb4Cu4O2(SO4)4⋅(Cu0.83R
Autor:
Alexander F. Khlebnikov, Olesya A. Tomashenko, Mikhail S. Novikov, Nikita I. Efimenko, Dar’ya V. Spiridonova
Publikováno v:
Organic Letters. 23:6362-6366
2H-Azirine-2-carbonyl azides undergo a rearrangement into derivatives of 2-(1H-tetrazol-1-yl)acetic acid when interacting with O- and S-nucleophiles at room temperature. The reaction is catalyzed by tertiary amines or hydrazoic acid. The reaction wit
Autor:
Vladimir V. Shilovskikh, Sergey V. Krivovichev, Alina R. Izatulina, Maria G. Krzhizhanovskaya, Dar’ya V. Spiridonova, Mikhail N. Murashko, Vladislav V. Gurzhiy
Publikováno v:
Journal of Geosciences. :249-259