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Metal-catalysed C–H bond activation and borylation
Transition metal-catalysed direct borylation of hydrocarbons via C–H bond activation has
received a remarkable level of attention as a popular reaction in the synthesis of …
received a remarkable level of attention as a popular reaction in the synthesis of …
First-row d-block element-catalyzed carbon–boron bond formation and related processes
SK Bose, L Mao, L Kuehn, U Radius… - Chemical …, 2021 - ACS Publications
Organoboron reagents represent a unique class of compounds because of their utility in
modern synthetic organic chemistry, often affording unprecedented reactivity. The …
modern synthetic organic chemistry, often affording unprecedented reactivity. The …
Trends in the usage of bidentate phosphines as ligands in nickel catalysis
AL Clevenger, RM Stolley, J Aderibigbe… - Chemical …, 2020 - ACS Publications
A critically important process in catalysis is the formation of an active catalyst from the
combination of a metal precursor and a ligand, as the efficacy of this reaction governs the …
combination of a metal precursor and a ligand, as the efficacy of this reaction governs the …
A decade advancement of transition metal-catalyzed borylation of aryl halides and sulfonates
This review describes the recent advancement of transition metal-catalyzed aromatic carbon-
boron bond construction processes. The efficacy of palladium, nickel and copper catalysis …
boron bond construction processes. The efficacy of palladium, nickel and copper catalysis …
Visible-light-induced Ni-catalyzed radical borylation of chloroarenes
A highly selective and general photoinduced C–Cl borylation protocol that employs [Ni
(IMes) 2](IMes= 1, 3-dimesitylimidazoline-2-ylidene) for the radical borylation of …
(IMes) 2](IMes= 1, 3-dimesitylimidazoline-2-ylidene) for the radical borylation of …
Nickel-catalyzed Suzuki–Miyaura couplings in green solvents
The nickel-catalyzed Suzuki–Miyaura coupling of aryl halides and phenol-derived
substrates with aryl boronic acids using green solvents, such as 2-Me-THF and tert-amyl …
substrates with aryl boronic acids using green solvents, such as 2-Me-THF and tert-amyl …
Additive-and metal-free, predictably 1, 2-and 1, 3-regioselective, photoinduced dual C–H/C–X borylation of haloarenes
We report herein a simple, additive-and metal-free, photoinduced, dual C–H/C–X borylation
of chloro-, bromo-, and iodoarenes. The reaction produces 1, 2-and 1, 3-diborylarenes on …
of chloro-, bromo-, and iodoarenes. The reaction produces 1, 2-and 1, 3-diborylarenes on …
Nickel-Catalyzed Borylation of Halides and Pseudohalides with Tetrahydroxydiboron [B2(OH)4]
Arylboronic acids are gaining increased importance as reagents and target structures in a
variety of useful applications. Recently, the palladium-catalyzed synthesis of arylboronic …
variety of useful applications. Recently, the palladium-catalyzed synthesis of arylboronic …
Efficient synthesis of aryl boronates via zinc-catalyzed cross-coupling of alkoxy diboron reagents with aryl halides at room temperature
A zinc (II)/NHC system catalyzes the borylation of aryl halides with diboron (4) reagents in
the presence of KOMe at rt. This transformation can be applied to a broad range of …
the presence of KOMe at rt. This transformation can be applied to a broad range of …
Hydride as a leaving group in the reaction of pinacolborane with halides under ambient grignard and barbier conditions. One-Pot synthesis of alkyl, aryl, heteroaryl …
JW Clary, TJ Rettenmaier, R Snelling… - The Journal of …, 2011 - ACS Publications
Grignard reagents (aliphatic, aromatic, heteroaromatic, vinyl, or allylic) react with 1 equiv of
4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane (pinacolborane, PinBH) at ambient temperature …
4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane (pinacolborane, PinBH) at ambient temperature …