1517-71-1

Upstream product

• 917-64-6 methyl magnesium iodide 
• 487-68-3 mesytaldehyde 
• 1667-01-2 2,4,6-Trimethylacetophenone 
• 1517-71-1 1-mesitylethanol 
• 97-72-3 2-Methylpropionic anhydride 
• 769-25-5 2,4,6-trimethylstyrene 
• 866418-04-4 chloroacetic acid 1-(2,4,6-trimethylphenyl)ethyl ester 
• 934631-25-1 rac-3-(3-pyridine)propionic acid 1-mesityl-ethyl ester 
• 75-07-0 acetaldehyde 
• 2633-66-1 2-mesitylmagnesium bromide 
• 917-54-4 methyllithium 
• 75-16-1 methylmagnesium bromide 
• 108-67-8 1,3,5-trimethyl-benzene 
• 67-63-0 isopropyl alcohol 

Downstream Products

• 51270-90-7 (R)-1-chloro-1-mesityl-ethane 
• 111357-65-4 (+/-)-phthalic acid mono-(1-mesityl-ethyl ester) 
• 86561-29-7 acetic acid-(1-mesityl-ethyl ester) 
• 3982-67-0 ethylmesitylene 
• 1517-71-1 (S)-1-(2,4,6-trimethylphenyl)ethanol 
• 2516-69-0 (R)-1-mesitylethanol 
• 84194-77-4 Acetic acid (S)-1-(2,4,6-trimethyl-phenyl)-ethyl ester 
• 1667-01-2 2,4,6-Trimethylacetophenone 
• 866418-04-4 chloroacetic acid 1-(2,4,6-trimethylphenyl)ethyl ester 
• 934631-25-1 rac-3-(3-pyridine)propionic acid 1-mesityl-ethyl ester 
• 1028432-18-9 C₂₄H₃₇NO₃SSi 
• 1195962-57-2 (E)-1-(1-mesitylethoxy)-2-methylpent-1-en-3-one 
• 1268070-61-6 (S)-1-mesitylethyl isobutyrate 

Relevant academic research and scientific papers

Novel N-coordinate half-sandwich ruthenium(II) arene complexes bearing sulfonamide fragments: Catalytic activities in the TH of acetophenone derivatives

Abstract The novel cationic N-coordinate ruthenium(II)/arene complexes (6-10) were prepared from the starting complex [RuCl2(p-cymene)]2 dimer. The structures of the [(p-cymene)RuLCl]Cl (L = N-arenesulfonyl-4,5-dimethyl-o-phenylenedi

Synthesis and catalytic activity of semiconducting p-cymene ruthenium 1,3,4-thiadiazole and 1,2,4-triazole complexes

The novel ruthenium(II) complexes containing 5-(pyridin-4-yl)-1,3,4- thiadiazol-2-amine(1) and 4-amino-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiol (2) ligands were synthesized and characterized by UV-Vis, IR, NMR, and elemental analysis. The complexes have

Catalytic transfer hydrogenation and anticancer activity of arene-ruthenium compounds incorporating bi-dentate precursors

Ruthenium based organometallic compounds are presently a subject of great attention as anticancer drugs and appear to work reasonably well on tumor cells. We develop a series of mononuclear arene-ruthenium compounds incorporating N,O and N,N bidentate lig

Ruthenium(II) carbonyl chloride complexes containing pyridine- functionalised bidentate N-heterocyclic carbenes: Synthesis, structures, and impact of the carbene ligands on catalytic activities

A series of new ruthenium(II) carbonyl chloride complexes with pyridine-functionalised N-heterocyclic carbenes [Ru(Py-NHC)(CO) 2Cl2], [Py-NHC = 3-methyl-1-(2-pyridyl)imidazol-2-ylidene, 1 (1a and 1b); 3-methyl-1-(2-picoyl)imidazol-2-

Preparation, characterization, and catalytic properties of ruthenium nitrosyl complexes with polypyrazolylmethane ligands

Ruthenium(II) nitrosyl complexes with polypyrazolylmethanes, [(Bpm)Ru(NO)Cl3] [Bpm = bis(1-pyrazolyl)methane, 1], [(Bpm*)Ru(NO)Cl3] [Bpm* = bis(3,5-dimethyl-1-pyrazolyl)methane, 2], [(Tpm)Ru(NO)Cl2][P

Synthesis, structures and catalytic activities of ruthenium(ii) carbonyl chloride complexes containing pyridine-functionalised N-heterocyclic carbenes

A series of ruthenium(ii) carbonyl chloride complexes with pyridine-functionalised N-heterocyclic carbenes, trans(Cl)- and cis(Cl)-[Ru(Py-NHC)(CO)2Cl2] [Py-NHC = 3-tert-butyl-1-(2-pyridyl)imidazol-2-ylidene, 1a and 1b; 3-n-butyl-1-(2

Quinoline-functionalized N-heterocyclic carbene complexes of iridium: Synthesis, structures and catalytic activities in transfer hydrogenation

Iridium complexes containing quinoline-functionalized N-heterocyclic carbene (NHC) ligands have been synthesized by the transmetalation route from silver carbene precursors. The silver complexes undergo a facile reaction with [Ir(COD)Cl]2 (COD

In situ catalytic activities of 1,3-dialkyltetrahydropyrimidinium salts/[RuCl2(p-cymene)]2 system for transfer hydrogenation reactions

Hydrogen-transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity. In the present study novel ruthenium carbene complexes were generated in situ and tested for their transfer hydrogena

Bis-N-heterocyclic carbene ruthenium(II) carbonyl complexes: Synthesis, structural characterization and catalytic activities in transfer hydrogenation of ketones

In this contribution, the synthesis and characterization of eight ruthenium(II) carbonyl complexes supported by chelating alkane-bridged bis-N-heterocyclic carbene ligands are reported. The products obtained are analyzed using infrared and NMR spectroscop

Applying Le Chatelier's Principle for a Highly Efficient Catalytic Transfer Hydrogenation with Ethanol as the Hydrogen Source

While isopropanol or formic acid derivatives are mainly applied as hydrogen sources in catalytic transfer hydrogenation reactions, there are only a few reports on the use of primary alcohols. In the present communication we report that ecologically benign and cheap ethanol can be applied with a ruthenium(II) that is completely stable against moisture and oxygen. Catalytic transfer hydrogenation is an equilibrium reaction. Therefore, a rapid removal of acetic aldehyde being formed as the product of ethanol oxidation is the key for high conversions. The reaction shows a broad substrate scope and allows the hydrogenation of ketones, aldehydes and imines.