Selective decarbonylation via transition-metal-catalyzed carbon–carbon bond cleavage
H Lu, TY Yu, PF Xu, H Wei - Chemical Reviews, 2020 - ACS Publications
Transition-metal-catalyzed decarbonylation via carbon–carbon bond cleavage is an
essential synthetic methodology. Given the ubiquity of carbonyl compounds, the selective …
essential synthetic methodology. Given the ubiquity of carbonyl compounds, the selective …
Recent advances in the synthesis and CF functionalization of gem-difluoroalkenes
X Zhang, S Cao - Tetrahedron Letters, 2017 - Elsevier
The gem-difluoroalkenes and related compounds have gained much attention from the
organic synthetic community due to their widespread applications as versatile fluorinated …
organic synthetic community due to their widespread applications as versatile fluorinated …
Synthesis of fluorinated compounds by Nickel-catalyzed defluorinative cross-coupling reactions
K Wang, W Kong - ACS Catalysis, 2023 - ACS Publications
Organofluorine compounds have attracted extensive attention in various industrial fields due
to their unique chemical and physical properties. Despite increasing demand in a wide …
to their unique chemical and physical properties. Despite increasing demand in a wide …
Site-selective cross-coupling of polyhalogenated arenes and heteroarenes with identical halogen groups
V Palani, MA Perea, R Sarpong - Chemical reviews, 2021 - ACS Publications
Methods to functionalize arenes and heteroarenes in a site-selective manner are highly
sought after for rapidly constructing value-added molecules of medicinal, agrochemical, and …
sought after for rapidly constructing value-added molecules of medicinal, agrochemical, and …
Selectivity of C–H activation and competition between C–H and C–F bond activation at fluorocarbons
O Eisenstein, J Milani, RN Perutz - Chemical Reviews, 2017 - ACS Publications
Partially fluorinated alkanes, arenes, and alkenes can be transformed by a variety of
transition metal and lanthanide systems. Although the C–H bond is weaker than the C–F …
transition metal and lanthanide systems. Although the C–H bond is weaker than the C–F …
Synthetic Advantages of Defluorinative C− F Bond Functionalization
LV Hooker, JS Bandar - Angewandte Chemie, 2023 - Wiley Online Library
Much progress has been made in the development of methods to both create compounds
that contain C− F bonds and to functionalize C− F bonds. As such, C− F bonds are becoming …
that contain C− F bonds and to functionalize C− F bonds. As such, C− F bonds are becoming …
Visible‐Light‐Induced Selective Defluoroborylation of Polyfluoroarenes, gem‐Difluoroalkenes, and Trifluoromethylalkenes
Fluorinated organoboranes serve as versatile synthetic precursors for the preparation of
value‐added fluorinated organic compounds. Recent progress has been mainly focused on …
value‐added fluorinated organic compounds. Recent progress has been mainly focused on …
Selective photocatalytic C–F borylation of polyfluoroarenes by Rh/Ni dual catalysis providing valuable fluorinated arylboronate esters
YM Tian, XN Guo, MW Kuntze-Fechner… - Journal of the …, 2018 - ACS Publications
A highly selective and general photocatalytic C–F borylation protocol that employs a
rhodium biphenyl complex as a triplet sensitizer and the nickel catalyst [Ni (IMes) 2](IMes= 1 …
rhodium biphenyl complex as a triplet sensitizer and the nickel catalyst [Ni (IMes) 2](IMes= 1 …
Ni-catalyzed borylation of aryl fluorides via C–F cleavage
XW Liu, J Echavarren, C Zarate… - Journal of the American …, 2015 - ACS Publications
A Ni-catalyzed borylation via C–F activation is described. This protocol is distinguished by a
wide scope, including unactivated fluoroarenes, without compromising its efficiency and …
wide scope, including unactivated fluoroarenes, without compromising its efficiency and …
Preparing (multi) fluoroarenes as building blocks for synthesis: nickel-catalyzed borylation of polyfluoroarenes via C–F bond cleavage
J Zhou, MW Kuntze-Fechner… - Journal of the …, 2016 - ACS Publications
The [Ni (IMes) 2]-catalyzed transformation of fluoroarenes into arylboronic acid pinacol
esters via C–F bond activation and transmetalation with bis (pinacolato) diboron (B2pin2) is …
esters via C–F bond activation and transmetalation with bis (pinacolato) diboron (B2pin2) is …