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665177 Aldrich

Chloro[tris(para-trifluoromethylphenyl)phosphine]gold(I)

99%

Synonym: [Tris(para-trifluoromethylphenyl)phosphine]gold(I) chloride

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Properties

Related Categories Catalysis and Inorganic Chemistry, Chemical Synthesis, Gold, Gold Catalysts, Gold Complexes More...
InChI Key   UNHMCLFZEQKHCQ-UHFFFAOYSA-M
assay   99%

Description

Packaging

1 g in glass bottle

250 mg in glass bottle

Application

Gold Catalysts — 21st Century ′Gold Rush′

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

DuPhos and BPE Phospholane Ligands

Asymmetric hydrogenation reactions represent the ideal process for the commercial manufacture of single-enantiomer compounds, because of the ease by which these robust procedures can be scaled up and...
Aldrich ChemFiles 2006, 6.8, 3.
Keywords: Addition reactions, Alkylations, Allylborations, Amidations, Aminations, Asymmetric catalysis, Asymmetric synthesis, Building blocks, Catalysis, Chemfiles, Crotylborations, Cycloadditions, Electronics, Hydrogenations, Ligands, Purification, Reductions, Reductive aminations, transformation

Gold Catalysis

Gold catalysis is playing an increasing role in organic synthesis for the facile construction of complex architectures not readily accessed by standard methods. Gold catalysts mediate unique C–C, C–O...
Aldrich ChemFiles 2007, 7.5, 10.
Keywords: Catalysis, Chemfiles, Enyne rearrangements, Heterocycle formation, Isomerizations, Methods, Organic synthesis, Rearrangements

Related Content

Gold Catalyst in Chemical Synthesis

Introduction Hashmi, Toste, Echavarren, and Haruta, among others, have fueled the advance of gold into the forefront of transition metal catalysis.1,2 Phosphine ligated gold(I) complexes have risen a...
Keywords: Asymmetric synthesis, Building blocks, Catalysis, Claisen rearrangement, Conia-Ene Reaction, Cyclizations, Cycloadditions, Cycloisomerizations, Cyclopropanations, Deprotonations, Ene reaction, Hydroaminations, Hydrogenations, Isomerizations, Ligands, Rautenstrauch rearrangements, Rearrangements, Reductions, Schmidt Reaction, Substitutions

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