Results 1 to 10 of about 2,853 (118)

Polymeric iridium catalysts for C–H borylation of arenes under batch and continuous flow conditions [PDF]

open access: yesCommunications Chemistry
Iridium-catalyzed direct C–H borylation of arenes has been extensively studied as an efficient method for synthesizing arylboronates. However, this transformation predominantly relies on homogeneous iridium catalysts, which are typically air-sensitive ...
Zhenzhong Zhang   +2 more
doaj   +2 more sources

Triazine-based cobalt pincer complex for regioselective C-H borylation of furans [PDF]

open access: yesScientific Reports
Selective C-H borylation of heteroarenes is a valuable strategy for accessing organoboron intermediates, with cobalt pincer complexes demonstrating the potential of first-row transition metals as efficient alternatives to precious-metal catalysts.
Dariusz Lewandowski, Grzegorz Hreczycho
doaj   +2 more sources

Ligand-enabled C–H borylation of diverse classes of arenes

open access: yesTetrahedron Chem, 2022
Here we report a new 6,6′-bipyridine based ligand framework for the iridium-catalysed regioselective ortho borylation of diverse classes of arenes containing different functional groups.
Md Emdadul Hoque   +7 more
doaj   +1 more source

Development of a New Methodology for Dearomative Borylation of Coumarins and Chromenes and Its Applications to Synthesize Boron-Containing Retinoids

open access: yesMolecules, 2023
Dearomative borylation of coumarins and chromenes via conjugate addition represents a relatively unexplored and challenging task. To address this issue, herein, we report a new and general copper (I) catalyzed dearomative borylation process to synthesize
Bhaskar C. Das   +4 more
doaj   +1 more source

Transition metal-free visible light photoredox-catalyzed remote C(sp3)−H borylation enabled by 1,5-hydrogen atom transfer

open access: yesCommunications Chemistry, 2023
The borylation of unreactive carbon-hydrogen bonds is a valuable method for transforming feedstock chemicals into versatile building blocks. Here, we describe a transition metal-free method for the photoredox-catalyzed borylation of unactivated C(sp3)−H ...
Beiqi Sun   +4 more
doaj   +1 more source

Photoelectrochemical oxidative C(sp3)−H borylation of unactivated hydrocarbons

open access: yesNature Communications, 2023
Organoboron compounds are of high significance in organic synthesis due to the unique versatility of boryl substituents to access further modifications.
Ping-Fu Zhong   +6 more
doaj   +1 more source

Pyridinium-catalyzed decarboxylative borylation of benzoyl peroxides

open access: yesGreen Synthesis and Catalysis, 2021
A pyridinium salt catalyzed radical borylation of benzoyl peroxides is reported herein. A range of benzoyl peroxides having different electronic properties were well compatible in this borylation reaction, delivering various arylboronates in good yields ...
Shuxian Zhu   +4 more
doaj   +1 more source

Arene C–H borylation strategy enabled by a non-classical boron cluster-based electrophile

open access: yesNature Communications, 2023
Electrophilic borylation of sterically hindered arenes is a challenging transformation. Here, authors report a metal-free electrophilic C–H borylation of hindered arenes using a boron cluster reagent producing valuable aryl boronic esters.
Sangmin Kim   +6 more
doaj   +1 more source

Updated Progress of the Copper-Catalyzed Borylative Functionalization of Unsaturated Molecules

open access: yesMolecules, 2023
Borylation has become a powerful method to synthesize organoboranes as versatile building blocks in organic synthesis, medicinal chemistry, and materials science.
Bingru Li   +5 more
doaj   +1 more source

Group-assisted purification (GAP) chemistry for the synthesis of Velcade via asymmetric borylation of N-phosphinylimines

open access: yesBeilstein Journal of Organic Chemistry, 2014
A new approach to the anticancer drug Velcade was developed by performing asymmetric borylation of an imine anchored with a chiral N-phosphinyl auxiliary.
Jian-bo Xie   +4 more
doaj   +1 more source

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