A comprehensive review of caged phosphines: synthesis, catalytic applications, and future perspectives

H Shet, U Parmar, S Bhilare, AR Kapdi - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
Phosphines have played an important role in the rapid rise of transition metal-catalysed
processes and with the possibility of fine-tuning the electronic and steric properties of these …

Synthetic methods for the generation and preparative application of benzyne

T Kitamura - Australian journal of chemistry, 2010 - CSIRO Publishing
Many methods have been developed for generating benzyne. Convenient and reliable
precursors extensively studied so far involve benzenediazonium-2-carboxylate and o …

Phosphines and related C–P bonded compounds

DW Allen - 2015 - books.rsc.org
This chapter covers the literature published during 2013 relating to the above area, apart
from a few papers from 2012 in less accessible journals which came to light in Chemical …

Oxygen-promoted PdCl 2-catalyzed ligand-free Suzuki reaction in aqueous media

C Liu, Q Ni, P Hu, J Qiu - Organic & Biomolecular Chemistry, 2011 - pubs.rsc.org
A simple and efficient protocol has been developed for the PdCl2-catalyzed ligand-free and
aerobic Suzuki reaction of aryl bromides or nitrogen-based heteroaryl bromides with …

Zwitterionic palladium complexes: room-temperature Suzuki–Miyaura cross-coupling of sterically hindered substrates in an aqueous medium

JY Lee, D Ghosh, JY Lee, SS Wu, CH Hu, SD Liu… - …, 2014 - ACS Publications
A series of new imidazolium chlorides were straightforwardly prepared from the reactions
between chloroacetone and imidazole derivatives. Deprotonation of the methylene proton …

Synthesis of 3-arylcoumarins via Suzuki-cross-coupling reactions of 3-chlorocoumarin

MJ Matos, S Vazquez-Rodriguez, F Borges… - Tetrahedron …, 2011 - Elsevier
A convenient, new, and effective protocol for a rapid synthesis of different substituted 3-
arylcoumarins is reported. The developed synthetic route involves Pd-catalyzed cross …

1, 4-Additions of tricyclic 1, 4-diphosphinines–a novel system to study σ-bond activation and π–π dispersion interactions

A Koner, Z Kelemen, G Schnakenburg… - Chemical …, 2018 - pubs.rsc.org
The dienic nature of the aromatic π-system in 1, 4-diphosphinines remains largely
unexplored to this day due to a lack of facile and efficient synthetic protocols. Recently …

2, 4, 6-Triphenylphosphinine and 2, 4, 6-triphenylposphabarrelene revisited: synthesis, reactivity and coordination chemistry

M Rigo, JAW Sklorz, N Hatje, F Noack, M Weber… - Dalton …, 2016 - pubs.rsc.org
The synthesis of 2, 4, 6-triphenylphosphinine has been revisited and a general protocol for
the preparation of such low-coordinate phosphorus compounds in good to excellent yields …

Pyridyl‐Functionalized 1‐Phosphabarrelene: Synthesis, Coordination Chemistry and Photochemical di‐π‐Methane Rearrangement

M Bruce, M Papke, AW Ehlers, M Weber… - … A European Journal, 2019 - Wiley Online Library
Abstract The [4+ 2] cycloaddition of 2‐(2′‐pyridyl)‐4, 6‐diphenyl‐λ3‐phosphinine with the
highly reactive dienophile hexafluoro‐2‐butyne has been studied and the first pyridyl …

In situ generated and stabilized Pd nanoparticles by N 2, N 4, N 6-tridodecyl-1, 3, 5-triazine-2, 4, 6-triamine (TDTAT) as a reactive and efficient catalyst for the Suzuki …

N Iranpoor, S Rahimi, F Panahi - RSC Advances, 2016 - pubs.rsc.org
In situ generated Pd nanoparticles in the presence of N2, N4, N6-tridodecyl-1, 3, 5-triazine-
2, 4, 6-triamine (TDTAT) were found to be an efficient catalyst for the Suzuki–Miyaura …