Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tatiana V. Strelkova"'
Autor:
Alexander S. Golubev, Petr N. Ostapchuk, Tatiana V. Strelkova, Nikolai D. Kagramanov, Kyrill Yu. Suponitsky, Rina U. Takazova, Nikolai D. Chkanikov
Publikováno v:
Organic & Biomolecular Chemistry. 20:6809-6820
New synthesis of 4-trifluoromethyl-2H-chromenes via the reaction of 2-(trifluoroacetyl)phenols with vinyltriphenylphosphonium chloride provides a reliable and prompt access to various substituted at the benzene ring 4-trifluoromethyl-2H-chromenes.
Autor:
Alexander S, Golubev, Petr N, Ostapchuk, Tatiana V, Strelkova, Nikolai D, Kagramanov, Kyrill Yu, Suponitsky, Rina U, Takazova, Nikolai D, Chkanikov
Publikováno v:
Organicbiomolecular chemistry. 20(34)
Substituted on the benzene ring 4-CF
Autor:
Zoya A. Starikova, Semen E. Nikolaev, Nadezhda E. Mysova, Elena G. Kononova, Fedor M. Dolgushin, Tatiana V. Strelkova, E. A. Petrushkina, Dmitry V. Khomishin
Publikováno v:
Journal of Organometallic Chemistry. 922:121373
Allyl alkylation of diethylmalonate with N-(2,7-dimethyl-2,7-octadien-1-yl)dialkylammonium iodide salts catalyzed by Pd (dba)2 without a phosphorus ligand and in the presence of NaH occurred with the predominant formation of a normal substitution pro
Publikováno v:
Organicbiomolecular chemistry. 16(39)
Dimethylamine adducts of triallyl-, triprenyl- and trans-cinnamyl(dipropyl)borane are effective reagents for mild homoallylation of primary amines with aqueous formaldehyde in MeOH without an inert atmosphere. A new concept is proposed for the explan
Publikováno v:
Organic letters. 20(12)
Triallylborane–amines adducts are effective stoichiometric allylating agents in the aminoallylation reaction of carbonyl compounds in methanol. Moreover, copper-catalyzed diastereoselective allylation of Ellman’s imine was achieved with triallylb
Autor:
Tatiana V. Strelkova, Syuzanna R. Harutyunyan, Nikolai S. Ikonnikov, Konstantin A. Kochetkov, Yuri N. Belokon, A. S. Saghiyan
Publikováno v:
Tetrahedron: Asymmetry, 12(3), 481-485. PERGAMON-ELSEVIER SCIENCE LTD
syn-(S)-β-Hydroxy-α-amino acids were synthesised stereoselectively via elaboration of the asymmetric aldol reactions of aldehydes with a chiral Ni(II)-(S)-BPB/glycine Schiff base complex in the presence of equimolar NaH in THF. The stereoselectivit
Autor:
Nikolai S. Ikonnikov, Konstantin A. Kochetkov, Syuzanna R. Harutyunyan, Yuri N. Belokon, A. S. Saghiyan, Tatiana V. Strelkova
Publikováno v:
ChemInform. 32
syn-(S)-β-Hydroxy-α-amino acids were synthesised stereoselectively via elaboration of the asymmetric aldol reactions of aldehydes with a chiral Ni(II)-(S)-BPB/glycine Schiff base complex in the presence of equimolar NaH in THF. The stereoselectivit