Evolution and Future of Hetero‐and Hydro‐Trifluoromethylations of Unsaturated C− C Bonds

S Kawamura, P Barrio, S Fustero… - Advanced Synthesis …, 2023 - Wiley Online Library
The difunctionalizative trifluoromethylation of unsaturated C− C bonds is a highly useful and
efficient method for the synthesis of trifluoromethyl compounds with attractive architectures …

Recent advances in graphene oxide catalyzed organic transformations

F Gao, S Zhang, Q Lv, B Yu - Chinese Chemical Letters, 2022 - Elsevier
Graphene oxide (GO), as a metal-free and readily available carbocatalyst, has been
extensively applied in catalytic organic transformations. This minireview aims to give an …

Electrooxidative dearomatization of biaryls: synthesis of tri-and difluoromethylated spiro [5.5] trienones

Y Zhang, C Ma, J Struwe, J Feng, G Zhu… - Chemical …, 2021 - pubs.rsc.org
Radical spirocyclization via dearomatization has emerged as an attractive strategy for the
rapid synthesis of structurally diverse spiro molecules. We report the use of electrochemistry …

Synthesis, structure elucidation, and in vitro pharmacological evaluation of novel polyfluoro substituted pyrazoline type sulfonamides as multi-target agents for …

C Yamali, HI Gul, C Kazaz, S Levent, I Gulcin - Bioorganic Chemistry, 2020 - Elsevier
Abstract A novel series of 4-(3-(difluorophenyl)-5-(dimethoxyphenyl)-4, 5-dihydropyrazol-1-
yl) benzenesulfonamides 1–8 were designed since sulfonamide and pyrazoline …

Electrochemical tandem fluoroalkylation-cyclization of vinyl azides: Access to trifluoroethylated and difluoroethylated N-heterocycles

L Lin, Q Liang, X Kong, Q Chen… - The Journal of Organic …, 2020 - ACS Publications
A transition-metal-and oxidant-free electrochemical strategy for radical fluoroalkylation of
vinyl azides was developed. The reaction was carried out under mild conditions by using …

Synthesis of enantioenriched fluorinated enol silanes enabled by asymmetric reductive coupling of fluoroalkylacylsilanes and 1, 3-enynes and Brook rearrangement

X Fang, S Wen, P Jin, W Bao, S Liu, H Cong… - ACS …, 2022 - ACS Publications
Fluorinated enol silanes are broadly useful in various synthetic transformations such as
Mukaiyama aldol, Michael, and Mannich reactions. However, previous methods to these …

Recent advances in the strategic incorporation of fluorine into new-generation taxoid anticancer agents

K Jayanetti, K Takemura, H Bendale, A Garg… - Journal of Fluorine …, 2023 - Elsevier
This account describes our recent progress on the strategic incorporation of fluorine and
organofluorine moieties into new-generation taxoid anticancer agents for medicinal …

Discovery of novel mRNA demethylase FTO inhibitors against esophageal cancer

B Qin, Q Bai, D Yan, F Yin, Z Zhu, C Xia… - Journal of Enzyme …, 2022 - Taylor & Francis
Abstract A series of 1, 2, 3-triazole analogues as novel fat mass and obesity-associated
protein (FTO) inhibitors were synthesised in this study. Among all 1, 2, 3-triazoles …

Pyrazole/pyrazoline as an excellent pharmacophore in the design of carbonic anhydrase inhibitors (2018–2022)

A Dorbabu - Archiv der Pharmazie, 2023 - Wiley Online Library
Carbonic anhydrase (CA) is a metalloenzyme that catalyzes the interconversion between
carbon dioxide and water and dissociated ions of carbonic acid. In addition, CA performs …

Understanding and controlling fluorinated diacyl peroxides and fluoroalkyl radicals in alkene fluoroalkylations

S Kawamura, M Sodeoka - The Chemical Record, 2023 - Wiley Online Library
The demand for practical methods for the synthesis of novel fluoroalkyl molecules is
increasing owing to their diverse applications. Our group has achieved efficient …