Organofluorine chemistry: Promising growth areas and challenges

LV Politanskaya, GA Selivanova… - Russian Chemical …, 2019 - iopscience.iop.org
Currently, the chemistry of organofluorine compounds is a leading and rapidly developing
area of organic chemistry. Fluorine present in a molecule largely determines its specific …

Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision

VP Ananikov, LL Khemchyan, YV Ivanova… - Russian Chemical …, 2014 - iopscience.iop.org
The challenges of the modern society and the growing demand of high-technology sectors
of industrial production bring about a new phase in the development of organic synthesis. A …

Olefin metathesis reactions with fluorinated substrates, catalysts, and solvents

S Fustero, A Simon-Fuentes, P Barrio… - Chemical …, 2015 - ACS Publications
Organofluorine compounds 1 have found increasing applications in key industrial fields
such as the pharmaceutical 2 and medicinal chemistry 3 or crop 4 and material sciences, 5 …

Recent Advances in the Cascade Cyclization Reactions of 1, 7‐Enynes

XS Zhang, YP Han, YM Liang - Advanced Synthesis & Catalysis, 2024 - Wiley Online Library
Elaborated molecular architectures, especially carbocyclic, heterocyclic, endocyclic, and
polycyclic molecular structures, serve as an important class of organic complexes because …

Развитие методологии современного селективного органического синтеза: получение функционализированных молекул с атомарной точностью

ВП Анаников, ЛЛ Хемчян, ЮВ Иванова… - Успехи химии, 2014 - mathnet.ru
Вызовы современного общества и нарастающие потребности высокотехнологичных
отраслей промышленного производства обусловливают новый этап в развитии …

Silaborative carbocyclizations of 1, 7-enynes. Diastereoselective preparation of chromane derivatives

YC Xiao, C Moberg - Organic letters, 2016 - ACS Publications
Palladium (0)-catalyzed carbocyclization of 1, 7-enynes mediated by (chlorodimethylsilyl)
pinacolborane proceeds with 1, 8-addition of the silicon and boron functions to give …

Lossen rearrangement by Rh (iii)-catalyzed C–H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives

DA Petropavlovskikh, DV Vorobyeva… - Organic & …, 2021 - pubs.rsc.org
A convenient and robust method for the preparation of new CF3-containing 2-quinolones
has been developed via a Rh (III)-catalyzed C–H activation/Lossen rearrangement …

Rhodium (iii)-catalyzed CF 3-carbenoid C–H functionalization of 6-arylpurines

DV Vorobyeva, MM Vinogradov… - Organic & …, 2018 - pubs.rsc.org
An efficient method for the CF3-carbenoid C–H functionalization of 6-arylpurines has been
developed. This protocol uses readily available methyl 3, 3, 3-trifluoro-2-diazopropionate as …

RhIII‐Catalyzed CF3‐Carbenoid C‐7 Functionalization of Indolines

IE Iagafarova, DV Vorobyeva… - European Journal of …, 2017 - Wiley Online Library
An efficient method for the CF3‐carbenoid C‐7 functionalization of N‐pyrimidylindolines has
been developed. This protocol uses readily available methyl 3, 3, 3‐trifluoro‐2 …

Synthesis of functionalized azepines via Cu (I)-catalyzed tandem amination/cyclization reaction of fluorinated allenynes

AN Philippova, DV Vorobyeva, PS Gribanov… - Molecules, 2022 - mdpi.com
An efficient method for the selective preparation of trifluoromethyl-substituted azepin-2-
carboxylates and their phosphorous analogues has been developed via Cu (I)-catalyzed …