Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis

LE Ehehalt, OM Beleh, IC Priest, JM Mouat… - Chemical …, 2024 - ACS Publications
Cross-electrophile coupling (XEC), defined by us as the cross-coupling of two different σ-
electrophiles that is driven by catalyst reduction, has seen rapid progression in recent years …

Late-Stage C(sp3)–H Methylation of Drug Molecules

E Mao, DWC MacMillan - Journal of the American Chemical …, 2023 - ACS Publications
Methyl groups are well understood to play a critical role in pharmaceutical molecules,
especially those bearing saturated heterocyclic cores. Accordingly, methods that install …

Engaging alkenes in metallaphotoredox: a triple catalytic, radical sorting approach to olefin-alcohol cross-coupling

Q Cai, IM McWhinnie, NW Dow, AY Chan… - Journal of the …, 2024 - ACS Publications
Metallaphotoredox cross-coupling is a well-established strategy for generating clinically
privileged aliphatic scaffolds via single-electron reactivity. Correspondingly, expanding …

Computationally Guided Ligand Discovery from Compound Libraries and Discovery of a New Class of Ligands for Ni-Catalyzed Cross-Electrophile Coupling of …

S Tcyrulnikov, AK Hubbell, D Pedro… - Journal of the …, 2024 - ACS Publications
Although screening technology has heavily impacted the fields of metal catalysis and drug
discovery, its application to the discovery of new catalyst classes has been limited. The …

Activation of N− O σ Bonds with Transition Metals: A Versatile Platform for Organic Synthesis and C− N Bonds Formation

U Todorović, R Martin Romero… - European Journal of …, 2023 - Wiley Online Library
N− O σ bonds containing compounds are versatile substrates for organic synthesis under
transition metal catalysis. Their ability to react through both polar (oxidative addition …

Internal Atom Exchange in Oxazole Rings: A Blueprint for Azole Scaffold Evaluation

D Spinnato, M Leutzsch, F Wang, J Cornella - Synlett, 2024 - thieme-connect.com
In this article, we provide a route to transform isoxazoles and oxadiazoles into the
corresponding pyrazoles and 1, 2, 4-triazoles in one step using catalytic amounts of an air …

Nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles

Y Zhao, C Wu, J Zhang, Y Gao, Z Yuan, X Li… - Organic Chemistry …, 2024 - pubs.rsc.org
A nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles has been
established for the efficient synthesis of (Z) N-aryl β-enamino esters. 5-Alkoxy/phenoxy …

Nickel-Catalyzed Three-Component Carboamination/Cyclization of Alkynes To Access 2, 3-Disubstituted Quinolines

Y Gao, J **ng, Y Huo, Q Chen, X Li, ASK Hashmi… - Organic …, 2025 - ACS Publications
Presented herein is a nickel-catalyzed chemo-and regioselective three-component tandem
carboamination and cyclization of terminal alkynes with organoboronic acids and anthranils …

ASNAr‐Active External Initiator that Enables Heterobifunctional Clickable Polythiophenes

V Lotocki, E Grignon, HA Mills, S Ye… - Macromolecular …, 2024 - Wiley Online Library
Abstract Poly (3‐hexylthiophene)(P3HT) is a well‐studied conjugated polymer; however, the
end‐group functionalization of these polymers is limited by fundamental synthetic …

Efficient nickel precatalysts for Suzuki-Miyaura cross-coupling of aryl chlorides and arylboronic acids under mild conditions

S Stewart, M John, M Nutt, J Offer, J Duczynski… - 2024 - chemrxiv.org
The synthesis and catalytic properties of Ni (II) complexes, with the general formula Ni
(NHC)[P (OR) 3](Ar) Cl is described. These complexes are air-stable and extremely effective …