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692468 Sigma-Aldrich

(R)-[(RuCl(DM-BINAP))2(μ-Cl)3][NH2Me2]

Synonym: Dimethylammonium dichlorotri(μ-chloro)bis[(R)-(+)-2,2′-bis[di(3,5-xylyl)phosphino]-1,1′-binaphthyl]diruthenate(II)

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Properties

Related Categories Asymmetric Synthesis, BINAPs, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Privileged Ligands and Complexes More...
InChI Key   LGSCCUXQQTYWAH-UHFFFAOYSA-M
storage temp.   2-8°C

Description

Application

Takasago Ligands and Complexes for Asymmetric Reactions

Packaging

50, 100 mg in glass bottle

Legal Information

Sold in collaboration with Takasago for reseach purposes only. JP Registration No. 3445074

Safety & Documentation

Safety Information

Symbol 
GHS02  GHS02
Signal word 
Warning
Hazard statements 
Precautionary statements 
RIDADR 
UN1325 - class 4.1 - PG 3 - Flammable solids, organic, n.o.s., HI: all
WGK Germany 
3

Documents

Certificate of Analysis

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Protocols & Articles

Articles

Takasago Ligands and Complexes for Asymmetric Reactions

The quest to find chiral catalysts capable of achieving high enantiomeric excess for a variety of asymmetric transformations has been an ongoing endeavor for the past 40 years. One of the most releva...
Keywords: Addition reactions, Arylations, Asymmetric synthesis, Catalysis, Hydrogenations, Ligands, transformation

Related Content

Takasago Ligands - Advantages and Applications

Introduction The quest to find chiral catalysts capable of achieving high enantiomeric excess for a variety of asymmetric transformations has been an ongoing endeavor for the past 40 years. One of th...
Keywords: Addition reactions, Applications, Arylations, Asymmetric synthesis, Building blocks, Catalysis, Epoxidations, Hydrogenations, Hydrosilylations, Ligands, Sharpless Epoxidation, transformation

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