The crucial role of silver(i)-salts as additives in C–H activation reactions: overall analysis of their versatility and applicability
Renato L. de Carvalho,
Emilay B. T. Diogo,
Simon L. Homölle
et al.
Abstract:This review discusses the important role of silver(i) salts as additives in transition-metal catalyzed C–H activation, and depicts the discussion about the current shift towards Ag-free procedures, as plausible and sustainable alternatives.
“…Given the crucial role of silver salts in arylating reactions with iodobenzene substrates, we conducted a screening of various silver salts. 34 The results indicated that silver trifluoroacetate (AgTFA) exhibited the best reaction efficiency. The replacement of Ag 2 CO 3 with AgTFA significantly improved the reaction yield, reaching 72% ( Table 1 , entry 8).…”
In this work, we present a design concept of introducing linear structures into the orthogonal configuration of 9,9'-spirobifluorene (SBF), aiming to enhance carrier mobilities while maintaining high triplet energies (ET),...
“…Given the crucial role of silver salts in arylating reactions with iodobenzene substrates, we conducted a screening of various silver salts. 34 The results indicated that silver trifluoroacetate (AgTFA) exhibited the best reaction efficiency. The replacement of Ag 2 CO 3 with AgTFA significantly improved the reaction yield, reaching 72% ( Table 1 , entry 8).…”
In this work, we present a design concept of introducing linear structures into the orthogonal configuration of 9,9'-spirobifluorene (SBF), aiming to enhance carrier mobilities while maintaining high triplet energies (ET),...
“…Meanwhile, the reduced Pd(0) species was oxidized to the Pd( ii ) catalyst with the assistance of a stoichiometric amount of silver, which was subsequently used in the next catalytic cycle. 20…”
Backbone-enabled site-selective modification of peptides with benzoquinone via Pd-catalyzed δ-C(sp2)-H functionalization has been achieved. The amide groups of peptides serve as internal directional groups, facilitating C-H functionalization through a kinetically...
“…1 As a consequence, various strategies have been developed for rapid access to intriguing fused compounds, among which transition metal (TM)-catalysed C–H functionalization represents a straightforward protocol due to its high efficiency and remarkable atom-/step-economy. 2 To date, a series of versatile directing groups (DGs) and coupling partners (CPs) have been discovered for addressing the synthesis of complex polycyclic ring-fused structures via a TM-catalysed C–H coupling/cyclization cascade involving the formation of multiple new bonds in a simple one-pot operation, illustrating that the combination of TM-catalysed C–H functionalization and the cascade strategy should be a viable tool for the efficient construction of fused heterocycles. 3…”
By defining the gem-difluorocyclopropenyl acetates as versatile coupling partners, we have realized the Rh(III)-catalyzed cascade C-H functionalization/[3+2] dipolar cycloaddition of azomethine imines, which delivered a variety of gem-difluorinated pentacyclic indenzopyrazolpyrazolone...
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