Iron‐catalysed hydrofunctionalisation of alkenes and alkynes
MD Greenhalgh, AS Jones, SP Thomas - ChemCatChem, 2015 - Wiley Online Library
The metal‐catalysed hydrofunctionalisation of alkenes and alkynes provides a convenient
and atom‐economic route to diversely functionalised products with control of regio‐, chemo …
and atom‐economic route to diversely functionalised products with control of regio‐, chemo …
Electrophilic activation of silicon–hydrogen bonds in catalytic hydrosilations
MC Lipke, AL Liberman‐Martin… - Angewandte Chemie …, 2017 - Wiley Online Library
Hydrosilation reactions represent an important class of chemical transformations and there
has been considerable recent interest in expanding the scope of these reactions by …
has been considerable recent interest in expanding the scope of these reactions by …
Rh (III)-and Ir (III)-catalyzed C–H alkynylation of arenes under chelation assistance
An efficient Rh (III)-and Ir (III)-catalyzed, chelation-assisted C–H alkynylation of a broad
scope of (hetero) arenes has been developed using hypervalent iodine-alkyne reagents …
scope of (hetero) arenes has been developed using hypervalent iodine-alkyne reagents …
Catalytic enantioselective functionalization of unactivated terminal alkenes
JR Coombs, JP Morken - Angewandte Chemie International …, 2016 - Wiley Online Library
Terminal alkenes are readily available functional groups which appear in α‐olefins
produced by the chemical industry, and they appear in the products of many contemporary …
produced by the chemical industry, and they appear in the products of many contemporary …
Catalysis by transition metal complexes of alkene silylation–recent progress and mechanistic implications
B Marciniec - Coordination Chemistry Reviews, 2005 - Elsevier
Many efficient stereo-and regio-selective methodologies for synthesis of substituted
vinylsilanes have been reported, involving mostly classical stoichiometric routes as well as …
vinylsilanes have been reported, involving mostly classical stoichiometric routes as well as …
Mechanistic studies of the rhodium-catalyzed direct C–H amination reaction using azides as the nitrogen source
Direct C–H amination of arenes offers a straightforward route to aniline compounds without
necessitating aryl (pseudo) halides as the starting materials. The recent development in this …
necessitating aryl (pseudo) halides as the starting materials. The recent development in this …
In situ determination of the active catalyst in hydrosilylation reactions using highly reactive Pt (0) catalyst precursors
J Stein, LN Lewis, Y Gao, RA Scott - Journal of the American …, 1999 - ACS Publications
The mechanism of hydrosilylation using the highly active precatalyst Karstedt's precatalyst
(Pt x (MvinylMvinyl) y, MvinylMvinyl= divinyltetramethyldisiloxane) was investigated using …
(Pt x (MvinylMvinyl) y, MvinylMvinyl= divinyltetramethyldisiloxane) was investigated using …
A review of recent progress in catalyzed homogeneous hydrosilation (hydrosilylation)
AK Roy - Advances in organometallic chemistry, 2007 - Elsevier
Publisher Summary This chapter discusses about compounds or complexes that facilitate
hydrosilation. The word ''true catalyst''is used where the actual catalytic species is positively …
hydrosilation. The word ''true catalyst''is used where the actual catalytic species is positively …
Phosphine-pyridyl and related ligands in synthesis and catalysis
P Espinet, K Soulantica - Coordination Chemistry Reviews, 1999 - Elsevier
This review summarizes the advances produced in the last 5 years in the use of mixed
ligands containing at least one phosphino and one pyridyl or related group (bipyridyl …
ligands containing at least one phosphino and one pyridyl or related group (bipyridyl …
Homogeneous catalytic reduction of CO 2 with hydrosilanes
Catalytic CO2 hydrosilylation is a thermodynamically favored chemical process that could be
potentially applied to large-scale transformations of this greenhouse gas. During the last …
potentially applied to large-scale transformations of this greenhouse gas. During the last …