Organic reactions in aqueous media with a focus on carbon− carbon bond formations: a decade update

CJ Li - Chemical Reviews, 2005 - ACS Publications
Organic syntheses are composed of two main types of reactions: Carbon-carbon bond
formations and functional group transformations. CC bond formation is the essence of …

Ruthenium complexes bearing bidentate Schiff base ligands as efficient catalysts for organic and polymer syntheses

R Drozdzak, B Allaert, N Ledoux, I Dragutan… - Coordination Chemistry …, 2005 - Elsevier
A concise overview is given on mononuclear and dinuclear, bidentate Schiff base ruthenium
complexes with different additional ligands and on their applications in various chemical …

Ruthenium-based olefin metathesis catalysts derived from alkynes

AM Lozano-Vila, S Monsaert, A Bajek… - Chemical …, 2010 - ACS Publications
The chemistry of vinylidene complexes displays a representative example of how highly
reactive, short-lived organic molecules may be effectively stabilized by coordination to …

CO Extrusion in homogeneous gold catalysis: Reactivity of gold acyl species generated through water addition to gold vinylidenes

J Bucher, T Stoesser, M Rudolph… - Angewandte Chemie …, 2015 - Wiley Online Library
Herein, we describe a new gold‐catalyzed decarbonylative indene synthesis. Synergistic σ,
π‐activation of diyne substrates leads to gold vinylidene intermediates, which upon addition …

Mechanistic investigation of the Ru-catalyzed hydroamidation of terminal alkynes

M Arndt, KSM Salih, A Fromm, LJ Goossen… - Journal of the …, 2011 - ACS Publications
The ruthenium-catalyzed hydroamidation of terminal alkynes has evolved to become a
broadly applicable tool for the synthesis of enamides and enimides. Depending on the …

[HTML][HTML] Recent advances in alkylidene carbene chemistry

RS Grainger, KR Munro - Tetrahedron, 2015 - Elsevier
Alkylidene carbenes, also known as alkenylidenes, are reactive intermediates in organic
chemistry. Their high reactivity necessitates generation and trapping in situ, but unlike many …

Internal alkyne isomerization to vinylidene versus stable π-Alkyne: theoretical and experimental study on the divergence of analogous Cp* Ru and TpRu systems

VK Singh, E Bustelo, I De Los Ríos… - …, 2011 - ACS Publications
The activation of internal alkynes by Cp* Ru and TpRu complexes gives respectively π-
alkyne and disubstituted vinylidene as stable species, even though both systems bear …

The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2004

JW Herndon - Coordination chemistry reviews, 2006 - Elsevier
This is a review of papers published in the year 2004 that focus on the synthesis, reactivity,
or properties of compounds containing a carbon–transition metal double or triple bond.

Reactivity of [TpRuCl(PTA)(PPh3)] with Alkynes and Propargylic Alcohols: Occurrence of Structurally Related Cationic vs Neutral Allenylidene Complexes with the …

S Bolano, MM Rodríguez-Rocha, J Bravo… - …, 2009 - ACS Publications
[TpRuCl (PTA)(PPh3)](1; PTA= 1, 3, 5-triaza-7-phosphaadamantane) reacts with
phenylacetylene, yielding the alkynyl complex [TpRu (C CPh)(PTA)(PPh3)](2) or the …

Ruthenium complexes containing bidentate Schiff base ligands as precursors of homogeneous and immobilized catalysts

F Ding, Y Sun, S Monsaert, R Drozdzak… - Current Organic …, 2008 - ingentaconnect.com
The paper presents recent work conducted in our group on the synthesis of a novel class of
homogeneous and immobilized Rucomplexes containing Schiff bases as O, N-bidentate …