Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nina K. Ratmanova"'
Autor:
Olga A. Ivanova, Vitaly V. Shorokhov, Ivan A. Andreev, Nina K. Ratmanova, Victor B. Rybakov, Elena D. Strel’tsova, Igor V. Trushkov
Publikováno v:
Molbank, Vol 2023, Iss 1, p M1604 (2023)
An 1,3-indanedione-derived donor–acceptor cyclopropane, bearing the ethoxymethyl-protected phenolic group at the ortho-position of the donor aryl substituent, has been synthesized using a reaction sequence involving the Knoevenagel condensation of
Externí odkaz:
https://doaj.org/article/af6a1ad4094a4167b32e38fbed07e1a0
Autor:
Ivan A. Andreev, Maksim A. Boichenko, Nina K. Ratmanova, Olga A. Ivanova, Irina I. Levina, Victor N. Khrustalev, Igor A. Sedov, Igor V. Trushkov
Publikováno v:
Advanced Synthesis & Catalysis. 364:2403-2415
Autor:
Tatiana A. Shestimerova, Ivan A. Andreev, Nina K. Ratmanova, Igor V. Trushkov, Alexey N. Kuznetsov, Andrei V. Shevelkov
Publikováno v:
Structural Chemistry.
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
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:
Ivan A. Andreev, Philip Barkawitz, Anu Jacob, Nina K. Ratmanova, Igor V. Trushkov, Daniel B. Werz
Publikováno v:
Synlett. 32:901-904
An easy and efficient route to obtain 2-amino-4,5-dihydrothiophenes is presented. A formal (3+2)-cycloaddition of donor–acceptor cyclopropanes and ammonium thiocyanate catalyzed by Yb(OTf)3 delivers the desired products in good to excellent yields.
Autor:
Nina K. Ratmanova, Ivan A. Andreev, André U. Augustin, Olga A. Ivanova, Igor V. Trushkov, Daniel B. Werz, Irina I. Levina, Victor N. Khrustalev
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie (International ed. in English) (2021) 60, 14, S. 7927-7934--Angew Chem Int Ed Engl--Angewandte Chemie International Edition--Angew Chem [Engl]--Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker., International edition.--1433-7851--1521-3773
Angewandte Chemie International Edition
Angewandte Chemie (International ed. in English) (2021) 60, 14, S. 7927-7934--Angew Chem Int Ed Engl--Angewandte Chemie International Edition--Angew Chem [Engl]--Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker., International edition.--1433-7851--1521-3773
We propose a new concept of the triple role of protic ionic liquids with nucleophilic anions: a) a regenerable solvent, b) a Brønsted acid inducing diverse transformations via general acid catalysis, and c) a source of a nucleophile. The efficiency
Autor:
I. F. Seregina, Dmitry S. Belov, Nina K. Ratmanova, Ivan A. Andreev, Anton M. Novoselov, Alexander V. Kurkin
Publikováno v:
Chemistry - A European Journal. 22:7262-7267
A facile one-pot approach based on a thermally induced metal- and solvent-free 5-endo-dig cyclization reaction of the amino propargylic alcohols in combination with Dess-Martin periodinane-promoted oxidative dearomatization of 4,5,6,7-tetrahydroindol
Autor:
Alexandre V. Leontiev, Nina K. Ratmanova, Olga A. Ivanova, Igor V. Trushkov, Ivan A. Andreev, Daria Momotova, Anton M. Novoselov
Publikováno v:
Tetrahedron. 76:131031
The principal methods for the synthesis of pyrrolizidine and indolizidine alkaloids and their unnatural analogs are described. Six main “strategic” approaches in regard to a key step forming azabicyclic skeleton are identified. Namely, these are:
Publikováno v:
Chemistry - A European Journal. 21:4141-4147
Herein we suggest an approach to oxygenated bicyclic amino acids based on an aza-Cope-Mannich rearrangement. Seven distinct amino acid scaffolds analogous to the natural products were prepared on a gram scale with precise control of stereochemistry.