Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

B2Pin2-Enabled Chemoselective Ni-Catalyzed Reductive Ar-Ar Coupling of Two Aryl Halides

View through CrossRef
A versatile Ni-catalyzed reductive coupling platform has been developed for the chemoselective cross-coupling of two distinct aryl (and heteroaryl) halides. The method employed B2Pin2 as a non-single-electron-transfer (non-SET) homogeneous reductant. The use of specific 2,9-dimethyl phenanthroline ligands (L1 and L2) and additives allows the protocol to be modulated, according to the electronic nature of the coupling partners. This includes the 1:1 coupling of electron-deficient aryl bromides with electron-rich aryl iodides, the coupling of two electronically similar (either rich or deficient) aryl halides, and reactions involving heteroaryl halides. These equimolar reactions afforded the biaryl scaffolds in moderate to good yields. Notably, a directing effect from nitrogen-containing heterocycles, such as 2-chloropyridine, 2chloropyrimidine and 8-bromoquinoline, further enhances chemoselectivity. Two proposals were implemented for the formation of a key Ar 1-LnNi I intermediate. One concerns Ni(I) reduction of Ar 1-LnNi II X generated from oxidative addition of Ar 1 X to LnNi 0 , the other emphasizes B2pin2-invoked reduction of Ar 1-LnNi III (X)2 generated from addition of Ar 1 X to LnNi I X. This cost-effective reductive system minimizes the need for an excess of one coupling partner in constructing biaryl scaffolds, and the mechanistic insights offer valuable guidance for the future development of cross-electrophile coupling methodologies.
Title: B2Pin2-Enabled Chemoselective Ni-Catalyzed Reductive Ar-Ar Coupling of Two Aryl Halides
Description:
A versatile Ni-catalyzed reductive coupling platform has been developed for the chemoselective cross-coupling of two distinct aryl (and heteroaryl) halides.
The method employed B2Pin2 as a non-single-electron-transfer (non-SET) homogeneous reductant.
The use of specific 2,9-dimethyl phenanthroline ligands (L1 and L2) and additives allows the protocol to be modulated, according to the electronic nature of the coupling partners.
This includes the 1:1 coupling of electron-deficient aryl bromides with electron-rich aryl iodides, the coupling of two electronically similar (either rich or deficient) aryl halides, and reactions involving heteroaryl halides.
These equimolar reactions afforded the biaryl scaffolds in moderate to good yields.
Notably, a directing effect from nitrogen-containing heterocycles, such as 2-chloropyridine, 2chloropyrimidine and 8-bromoquinoline, further enhances chemoselectivity.
Two proposals were implemented for the formation of a key Ar 1-LnNi I intermediate.
One concerns Ni(I) reduction of Ar 1-LnNi II X generated from oxidative addition of Ar 1 X to LnNi 0 , the other emphasizes B2pin2-invoked reduction of Ar 1-LnNi III (X)2 generated from addition of Ar 1 X to LnNi I X.
This cost-effective reductive system minimizes the need for an excess of one coupling partner in constructing biaryl scaffolds, and the mechanistic insights offer valuable guidance for the future development of cross-electrophile coupling methodologies.

Related Results

A Widely Applicable Dual-Catalytic System for Cross-Electrophile Coupling
A Widely Applicable Dual-Catalytic System for Cross-Electrophile Coupling
A new dual catalytic system for cross-electrophile coupling reactions between aryl and alkyl halides that features a Ni catalyst, a Co co-catalyst, and a mild homogeneous reductan...
Mononuclear Palladium(I) Aryl Complexes Performs Cross-Coupling Reactions with Organic Halides
Mononuclear Palladium(I) Aryl Complexes Performs Cross-Coupling Reactions with Organic Halides
Mononuclear Pd(I) species represent the least understood Pd intermediates in Pd-catalyzed reactions and isolable complexes of the type are exceedingly rare. Herein, we report the s...
Bis(pinacolato)diboron-Enabled Ni-Catalyzed Reductive Coupling of Alkyl with Aryl/Vinyl Electrophiles
Bis(pinacolato)diboron-Enabled Ni-Catalyzed Reductive Coupling of Alkyl with Aryl/Vinyl Electrophiles
The chemistry herein stresses the use of economic and environmentally friendly (bispinacolato)diboron, as the non-metallic reductant that enables the reductive cross-coupling of al...
Ullmann Coupling
Ullmann Coupling
Abstract This reaction is a copper‐promoted reductive coupling between aryl halides to form biaryls and is generally referred to as the Ullmann coupling. The study finds ...
Biological Activity, Apoptotic Induction and Cell Cycle Arrest of New Hydrazonoyl Halides Derivatives
Biological Activity, Apoptotic Induction and Cell Cycle Arrest of New Hydrazonoyl Halides Derivatives
Background:The hydrazonoyl halides are presently an important target in the field of medicinal chemistry. The interest in the chemistry of hydrazonoyl halides is a consequence of t...
Transition-Metal-Catalyzed Direct Arylation of Ammonia
Transition-Metal-Catalyzed Direct Arylation of Ammonia
AbstractIn the past few decades, transition-metal-catalyzed direct amination of aryl halides with ammonia has attracted significant attention from chemists because of its broad sub...
Suzuki Coupling
Suzuki Coupling
Abstract This reaction is a palladium‐catalyzed cross‐coupling between an aryl or vinyl halide (or its equivalents and pseudo‐ halide...
Pushing steric limits in osmium(IV) tetraaryl complexes
Pushing steric limits in osmium(IV) tetraaryl complexes
Investigations into the reactivity, properties, and applications of osmium(IV) tetraaryl complexes have been hampered by their low yielding syntheses from volatile and toxic OsO4 (...

Back to Top