Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Anton S. Makarov"'
Autor:
Alexander A. Fadeev, Alexey O. Chagarovskiy, Anton S. Makarov, Irina I. Levina, Olga A. Ivanova, Maxim G. Uchuskin, Igor V. Trushkov
Publikováno v:
Molecules, Vol 25, Iss 23, p 5748 (2020)
A simple general method for the synthesis of 1-acyl-2-(ortho-hydroxyaryl)cyclopropanes, which belong to the donor–acceptor cyclopropane family, has been developed. This method, based on the Corey–Chaykovsky cyclopropanation of 2-hydroxychalcones,
Externí odkaz:
https://doaj.org/article/fa7e95aef6c748059dfd911ce5ebb5e7
Publikováno v:
Organic Chemistry Frontiers. 9:737-744
We report the divergent synthesis of benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans using the concept of extended Corey–Chaykovsky reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47ef0d38f44312c884c4e1617b73441e
https://doi.org/10.1039/d1qo01646f
https://doi.org/10.1039/d1qo01646f
Publikováno v:
Organic Chemistry Frontiers.
A metal- and additive-free reaction of easily accessible N-acylpyridinium iodides, methylvinyl ketones and amines provides access to meta-substituted anilines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcefa78e8dcc5be3b2ccd38836e3aaa1
https://doi.org/10.1039/d3qo00583f
https://doi.org/10.1039/d3qo00583f
Autor:
Vladimir T. Abaev, Maxim G. Uchuskin, Igor V. Trushkov, Anton S. Makarov, Anton A. Merkushev, Pavel M. Shpuntov
Publikováno v:
European Journal of Organic Chemistry. 2021:1274-1285
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56df91c84988e17411c5e7de13957af3
https://doi.org/10.1002/ejoc.202001608
https://doi.org/10.1002/ejoc.202001608
Publikováno v:
Organic Chemistry Frontiers. 8:6553-6560
Furyl-tethered O-acetyl oximes undergo a rearrangement to yield densely substituted pyrroles in the presence of FeCl3·6H2O. The reactivity of a furan ring resembles the behaviour of an activated olefin with a formal leaving group that reacts with el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9475582f0ec4392e052bad362df6055c
https://doi.org/10.1039/d1qo01281a
https://doi.org/10.1039/d1qo01281a
Publikováno v:
The Journal of organic chemistry. 86(23)
The convergent one-pot method toward trisubstituted furans has been developed. The key transformation behind the synthetic protocol comprises the cascade acid-catalyzed conjugated addition of furans to commercially available or easily accessible α,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2f2f8cb13a46abef8f245420d952a1
https://pubmed.ncbi.nlm.nih.gov/34784209
https://pubmed.ncbi.nlm.nih.gov/34784209
Autor:
Vladimir T. Abaev, Maxim G. Uchuskin, Anna E. Kekhvaeva, Anton S. Makarov, Petrakis N. Chalikidi, Igor V. Trushkov
Publikováno v:
Synthesis. 51:3747-3757
The Brönsted acid-catalyzed cascade synthesis of densely substituted benzofurans from easily available salicyl alcohols and biomass-derived furans has been developed. The disclosed sequence includes the intermediate formation of 2-(2-hydroxybenzyl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0fb60f95ceff0ba0482c957d394c326
https://doi.org/10.1055/s-0039-1690000
https://doi.org/10.1055/s-0039-1690000
Publikováno v:
Synthesis. 50:3059-3086
Recent developments on the transformations of furans under oxidative conditions toward the total synthesis of complex natural compounds are discussed. Reactions and methods are classified according to the type of oxidant used. Comparisons are then ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dd6c9f0760f0e1d82681b50f1bc3876
https://doi.org/10.1055/s-0037-1610021
https://doi.org/10.1055/s-0037-1610021
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:1286-1293
A simple method for the synthesis of 2-(3-oxoalkyl)furan derivatives based on conjugate addition of 2-substituted furans to various α,β-unsaturated carbonyl compounds in the presence of copper(II) bromide as catalyst was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::546375ccc6bf4ec4407d718f1edf03ed
https://doi.org/10.1007/s10593-018-2206-1
https://doi.org/10.1007/s10593-018-2206-1
Autor:
Danny Price, Anna E. Kekhvaeva, Anton S. Makarov, Maxim G. Uchuskin, Igor V. Trushkov, Christopher J. J. Hall
Publikováno v:
Tetrahedron. 73:7042-7053
A CuBr2-catalyzed alkylation of furans with a broad scope of benzyl alcohols and benzaldehydes is reported. Reaction proceeds efficiently under mild reaction conditions requiring no inert atmosphere or other precautions. Moreover, it is shown that Cu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33f2b98d8b6a5656141d0b5892338211
https://doi.org/10.1016/j.tet.2017.10.054
https://doi.org/10.1016/j.tet.2017.10.054