Recent advances in the Suzuki–Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media

SE Hooshmand, B Heidari, R Sedghi, RS Varma - Green Chemistry, 2019 - pubs.rsc.org
The ever-increasing interest in the Suzuki–Miyaura cross-coupling reaction (SMR) and its
applications, with more than 40 years of history, has increased exponentially in the last …

Schiff base-derived homogeneous and heterogeneous palladium catalysts for the Suzuki–Miyaura reaction

P Das, W Linert - Coordination Chemistry Reviews, 2016 - Elsevier
The ligand-assisted palladium (Pd)-catalyzed Suzuki–Miyaura cross-coupling reaction is
one of the most attractive protocols in organic chemistry and phosphines have been …

Bio‐actives of betel leaf (Piper betle L.): A comprehensive review on extraction, isolation, characterization, and biological activity

M Madhumita, P Guha, A Nag - Phytotherapy Research, 2020 - Wiley Online Library
Piper betle L., belonging to Piperaceae family, known as a traditional herbal medicinal plant
and used for several health benefits in Asian countries. Currently, demand for its products …

Synthesis of Biaryls via Ligand‐Free Suzuki–Miyaura Cross‐Coupling Reactions: A Review of Homogeneous and Heterogeneous Catalytic Developments

I Hussain, J Capricho, MA Yawer - Advanced Synthesis & …, 2016 - Wiley Online Library
This review describes the recent developments in the field of Suzuki–Miyaura cross‐
coupling reaction, in particular with regard to ligand‐free catalysis. The catalysts outlined …

Ashes from organic waste as reagents in synthetic chemistry: A review

K Venkateswarlu - Environmental Chemistry Letters, 2021 - Springer
The decline of fossil-and ore-based materials is calling for more recycling of waste into new
materials. Here, I review the recycling of ashes from biomass into reagents for chemical …

Disintegrable n‐type Electroactive Terpolymers for high‐performance, transient organic electronics

H Park, Y Kim, D Kim, S Lee, FS Kim… - Advanced Functional …, 2022 - Wiley Online Library
Degradable organic semiconductors have significant potential for transient and biomedical
organic electronics, but there have been only a few studies on fully degradable conjugated …

Facile synthesis of Pd@ graphene nanocomposites with enhanced catalytic activity towards Suzuki coupling reaction

M Khan, MR Shaik, SF Adil, M Kuniyil, M Ashraf… - Scientific …, 2020 - nature.com
A facile and chemical specific method to synthesize highly reduced graphene oxide (HRG)
and Pd (HRG@ Pd) nanocomposite is presented. The HRG surfaces are tailored with amine …

Ligand‐Free Bioinspired Suzuki–Miyaura Coupling Reactions using Aryltrifluoroborates as Effective Partners in Deep Eutectic Solvents

G Dilauro, SM García, D Tagarelli, P Vitale… - …, 2018 - Wiley Online Library
Abstract Pd‐catalyzed Suzuki–Miyaura cross‐coupling between (hetero) aryl halides (Cl, Br,
I) and versatile, moisture‐stable mono‐and bifunctional potassium aryltrifluoroborates …

Palladium-scavenging self-assembled hybrid hydrogels–reusable highly-active green catalysts for Suzuki–Miyaura cross-coupling reactions

P Slavík, DW Kurka, DK Smith - Chemical science, 2018 - pubs.rsc.org
A hybrid hydrogel based on 1, 3: 2, 4-dibenzylidene sorbitol (DBS) modified with acyl
hydrazides combined with agarose was used for in situ reduction and binding of palladium …

A Pd/Cu-Free magnetic cobalt catalyst for C–N cross coupling reactions: Synthesis of abemaciclib and fedratinib

Z Khorsandi, AR Hajipour, MR Sarfjoo, RS Varma - Green Chemistry, 2021 - pubs.rsc.org
Herein, the synthesis of a nano-catalytic system comprising magnetic nanoparticles as the
core and edible natural ligands bearing functional groups as supports for cobalt species is …