Taking into account the vast arrays of fluorinated motifs known, 11 this review will be limited
to the monofluorination of organic compounds, ie, synthetic methods allowing the …

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 …

The introduction of a monofluoromethyl moiety has undoubtedly become a very important
area of research in recent years. Owing to the beneficial properties of organofluorine …

Monofluoroalkenes have found wide application in organic chemistry, medicinal chemistry,
and materials science. This review summarizes the most recent advances made regarding …

Abstract gem‐Heteroatom‐substituted fluoroalkenes have received little attention despite
their great potential in medicinal chemistry or in fine chemistry. Indeed, due to the electronic …

The Horner-Wadsworth-Emmons reaction is one of the most reliable and widespread
synthetic tools for the stereocontrolled construction of ethylenic bonds. The versatility of the …

A new highly efficient method for the synthesis of 2-fluoro-2-nitrostyrenes was described.
Radical nitration of readily available 2-bromo-2-fluorostyrenes with Fe (NO3) 3· 9H2O …

A general method for the synthesis of substituted indolizines by copper (II) acetate-promoted
oxidative [3+ 2]-annulation of α-fluoronitroalkenes with in situ generated pyridinium ylides …

An efficient route to pyrazolo [1, 5-a] pyridines by Cu (OAc) 2-promoted oxidative [3+ 2]-
annulation of nitroalkenes with in situ generated pyridinium imines is developed. The …

A copper-catalyzed, redox-neutral cascade difluoroalkylation/5-endo annulation/β-fluorine
cleavage of ynones is developed, providing a direct and stereoselective method to access …