Selected Copper‐Based Reactions for C− N, C− O, C− S, and C− C Bond Formation

S Bhunia, GG Pawar, SV Kumar… - Angewandte Chemie …, 2017 - Wiley Online Library
Metal‐catalyzed cross‐coupling reactions belong to the most important transformations in
organic synthesis. Copper catalysis has received great attention owing to the low toxicity …

Carbon trifluoromethylation reactions of hydrocarbon derivatives and heteroarenes

C Alonso, E Martinez de Marigorta, G Rubiales… - Chemical …, 2015 - ACS Publications
Fluorine has emerged as a “magic element” in medicinal chemistry, crop, and materials
science. 1 Although fluorine is the most abundant halogen in the earth's crust, it is contained …

Good partnership between sulfur and fluorine: sulfur-based fluorination and fluoroalkylation reagents for organic synthesis

C Ni, M Hu, J Hu - Chemical Reviews, 2015 - ACS Publications
Fluorine, often called as “a small atom with a big ego”, 1 lies in the second row and the 17th
column in the periodic table of the chemical elements. This unique position in the periodic …

Electrophotochemical synthesis facilitated trifluoromethylation of arenes using trifluoroacetic acid

J Qi, J Xu, HT Ang, B Wang, NK Gupta… - Journal of the …, 2023 - ACS Publications
The trifluoromethyl (CF3) group is an essential moiety in medicinal chemistry due to its
unique physicochemical properties. While trifluoroacetic acid (TFA) is an inexpensive and …

Application of Langlois' reagent in trifluoromethylation reactions

C Zhang - Advanced Synthesis & Catalysis, 2014 - Wiley Online Library
The incorporation of a trifluoromethyl (CF3) group into organic compounds is of great
importance in pharmaceutical, agricultural, and materials science. Trifluoromethylation …

Pushing the boundaries of C–H bond functionalization chemistry using flow technology

S Govaerts, A Nyuchev, T Noel - Journal of Flow Chemistry, 2020 - Springer
C–H functionalization chemistry is one of the most vibrant research areas within synthetic
organic chemistry. While most researchers focus on the development of small-scale batch …

Lewis Acid–Base Interaction‐Controlled ortho‐Selective C−H Borylation of Aryl Sulfides

HL Li, Y Kuninobu, M Kanai - Angewandte Chemie, 2017 - Wiley Online Library
An iridium/bipyridine‐catalyzed ortho‐selective C− H borylation of aryl sulfides was
developed. High ortho‐selectivity was achieved by a Lewis acid–base interaction between a …

3-Position-Selective C–H trifluoromethylation of pyridine rings based on nucleophilic activation

R Muta, T Torigoe, Y Kuninobu - Organic letters, 2022 - ACS Publications
The first example of the 3-position-selective C (sp2)–H trifluoromethylation of pyridine rings
was established. 3-Position-selective trifluoromethylation was achieved by the nucleophilic …

Photochemical [2+ 2] Cycloaddition of Alkynyl Boronates

OS Liashuk, OO Grygorenko… - … A European Journal, 2023 - Wiley Online Library
Abstract A photochemical [2+ 2] cycloaddition of alkynyl boronates and maleimides is
reported. The developed protocol provided 35–70% yield of maleimide‐derived …

[HTML][HTML] CF3SO2X (X= Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-,-sulfinyl-and-sulfonylation. Part 1: Use of CF3SO2Na

H Guyon, H Chachignon… - Beilstein Journal of …, 2017 - beilstein-journals.org
Abstract Sodium trifluoromethanesulfinate, CF 3 SO 2 Na, and trifluoromethanesulfonyl
chloride, CF 3 SO 2 Cl, are two popular reagents that are widely used for the direct …