Immobilization of N-heterocyclic carbene compounds: a synthetic perspective

R Zhong, AC Lindhorst, FJ Groche… - Chemical Reviews, 2017 - ACS Publications
Over the course of the past 15 years the success story of N-heterocyclic carbene (NHC)
compounds in organic, inorganic, and organometallic chemistry has been extended to …

Recent developments in palladium catalysed carbonylation reactions

ST Gadge, BM Bhanage - RSC Advances, 2014 - pubs.rsc.org
Recently, carbonylation reactions have gained considerable interest as they are becoming a
versatile tool in the synthesis of pharmaceuticals, agrochemicals and their intermediates …

Ex Situ Generation of Stoichiometric and Substoichiometric 12CO and 13CO and Its Efficient Incorporation in Palladium Catalyzed Aminocarbonylations

P Hermange, AT Lindhardt, RH Taaning… - Journal of the …, 2011 - ACS Publications
A new technique for the ex situ generation of carbon monoxide (CO) and its efficient
incorporation in palladium catalyzed carbonylation reactions was achieved using a simple …

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 …

Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@ Pd NPs supported on carbon nanotubes

L Nan, C Yalan, L Jixiang, O Dujuan, D Wenhui… - RSC …, 2020 - pubs.rsc.org
In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@ Pd/CNT) was
synthesized by modifying CNTs using Ni@ Pd core–shell nanoparticles (NPs). Ni@ Pd/CNT …

Suzuki-Miyaura cross-coupling in acylation reactions, scope and recent developments

M Blangetti, H Rosso, C Prandi, A Deagostino… - Molecules, 2013 - mdpi.com
Since the first report and due to its handiness and wide scope, the Suzuki-Miyaura (SM)
cross coupling reaction has become a routine methodology in many laboratories worldwide …

ppm level supported Pd-catalyzed carbonylative Suzuki–Miyaura cross-coupling of aryl iodides using oxalic acid as CO source

P Mehara, P Sharma, AK Sharma, P Das - Molecular Catalysis, 2023 - Elsevier
Polystyrene supported palladium (Pd@ PS) catalyzed cost-efficient and sustainable protocol
for carbonylative Suzuki-Miyaura cross-coupling (C-SMCC) reaction has been reported …

Palladacycle-Catalyzed Carbonylative Suzuki–Miyaura Coupling with High Turnover Number and Turnover Frequency

P Gautam, BM Bhanage - The Journal of Organic Chemistry, 2015 - ACS Publications
This work reports the carbonylative Suzuki–Miyaura coupling of aryl iodides catalyzed by
palladacycles. More importantly, the palladacycles have been used to generate high …

PS-Pd–NHC: an efficient and heterogeneous recyclable catalyst for direct reductive amination of carbonyl compounds with primary/secondary amines in aqueous …

DB Bagal, RA Watile, MV Khedkar, KP Dhake… - Catalysis Science & …, 2012 - pubs.rsc.org
A highly efficient polymer supported palladium-N–heterocyclic carbene (PS-Pd–NHC)
catalytic system has been developed for direct reductive amination (DRA) of carbonyl …

Aminocarbonylation of aryl iodides with primary and secondary amines in aqueous medium using polymer supported palladium-N-heterocyclic carbene complex as …

ZS Qureshi, SA Revankar, MV Khedkar, BM Bhanage - Catalysis today, 2012 - Elsevier
Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to
corresponding amides using polymer supported palladium-N-heterocyclic carbene complex …