Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update

D Bhattacherjee, M Rahman, S Ghosh… - Advanced Synthesis …, 2021 - Wiley Online Library
Transition metals have been an indispensable component of modern catalysis and among
these palladium is the top‐ranked choice of chemists as a catalyst. After the several …

Ortho CH Acylation of Aryl Iodides by Palladium/Norbornene Catalysis

Z Dong, J Wang, Z Ren, G Dong - Angewandte Chemie, 2015 - Wiley Online Library
Ortho CH Acylation of Aryl Iodides by Palladium/Norbornene Catalysis - Dong - 2015 -
Angewandte Chemie - Wiley Online Library Skip to Article Content Skip to Article Information …

Recent Progress in the Radical α-C (sp 3)–H Functionalization of Ketones

JZ Li, WK Zhang, GP Ge, H Zheng… - Organic & Biomolecular …, 2021 - pubs.rsc.org
The direct use structurally simple ketones as α-ketone radical sources for α-C (sp3)–H
functionalization is a sustainable and powerful approach for constructing complex and …

Palladium-catalyzed Suzuki–Miyaura cross-coupling of amides via site-selective N–C bond cleavage by cooperative catalysis

G Meng, S Shi, M Szostak - Acs Catalysis, 2016 - ACS Publications
Palladium-catalyzed Suzuki–Miyaura cross-coupling of primary benzamides enabled by a
merger of site-selective N, N-di-Boc-activation and cooperative catalysis via N–C bond …

Nickel-Catalyzed Diaryl Ketone Synthesis by N–C Cleavage: Direct Negishi Cross-Coupling of Primary Amides by Site-Selective N,N-Di-Boc Activation

S Shi, M Szostak - Organic letters, 2016 - ACS Publications
A general Negishi acylation of primary amides enabled by a combination of site-selective N,
N-di-Boc activation and nickel catalysis is reported for the first time. The reaction is promoted …

Efficient Synthesis of Diaryl Ketones by Nickel‐Catalyzed Negishi Cross‐Coupling of Amides by Carbon–Nitrogen Bond Cleavage at Room Temperature Accelerated …

S Shi, M Szostak - Chemistry–A European Journal, 2016 - Wiley Online Library
The first Negishi cross‐coupling of amides for the synthesis of versatile diaryl ketones by
selective C− N bond activation under exceedingly mild conditions is reported. The cross …

Organocatalytic C–H bond arylation of aldehydes to bis-heteroaryl ketones

QY Toh, A McNally, S Vera, N Erdmann… - Journal of the …, 2013 - ACS Publications
An organocatalytic aldehyde C–H bond arylation process for the synthesis of complex
heteroaryl ketones has been developed. By exploiting the inherent electrophilicity of …

Synthesis of Z-alkenes via visible light promoted photocatalytic E→ Z isomerization under metal-free conditions

W Cai, H Fan, D Ding, Y Zhang, W Wang - Chemical Communications, 2017 - pubs.rsc.org
A green approach for the synthesis of thermodynamically less stable Z-alkenes has been
presented through the exploration of visible light promoted photocatalytic E-to-Z …

Depolymerization of robust polyetheretherketone to regenerate monomer units using sulfur reagents

Y Minami, N Matsuyama, Y Takeichi… - Communications …, 2023 - nature.com
Super engineering plastics, high-performance thermoplastic resins such as
polyetheretherketone, and polyphenylene sulfide have been utilized in industries, owing to …

General method for the Suzuki–Miyaura cross-coupling of primary amide-derived electrophiles enabled by [Pd (NHC)(cin) Cl] at room temperature

P Lei, G Meng, Y Ling, J An, SP Nolan, M Szostak - Organic letters, 2017 - ACS Publications
A general, highly selective method for the room temperature Suzuki–Miyaura cross-coupling
of commonly encountered primary benzamides is reported. A combination of site-selective …