62860-42-8

Upstream product

• 52340-78-0 (R,R)-hydroxybenzoin 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 24894-88-0 threo-1,2-diphenyl-1,2-bis(trimethylsilyl)ethane 
• 74-88-4 methyl iodide 
• 645-49-8 cis-stilben 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 116117-99-8 1,2-diphenyl-1-methoxy-2-phenylselenenyl ethane dichloride, threo 
• 116117-92-1 1,2-diphenyl-1-methoxy-2-phenylselenenyl ethane 
• 3524-62-7 benzoin monomethyl ether 
• 2325-10-2 (S,S)-hydrobenzoin 
• 116117-92-1 1,2-diphenyl-1-methoxy-2-phenylselenenyl ethane 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 18586-58-8 1,2-bis(trimethylsilyl)-1,2-diphenylethane 

Relevant academic research and scientific papers

A chiral ligand mediated aza-conjugate addition strategy for the enantioselective synthesis of β-amino esters that contain hydrogenolytically sensitive functionality

Aza-conjugate addition of the lithium anion of N-trimethylsilyl-p-methoxybenzylamine to tert-butyl enoate acceptors, in the presence of a stoichiometric amount of enantiopure 1,2-dimethoxy-1,2-diphenylethane and excess trimethylsilyl chloride, affords ter

Catalytic asymmetric bromine-lithium exchange: A new tool to build axial chirality

We present here the first catalytic desymmetrization of the 2,2′,6,6′-tetrabromobiphenyl 1 and analogues, by a bromine-lithium exchange catalyzed by either diamines or diether derivatives (0.5 equiv.), yielding axially chiral compounds in high yield (up to 89%) and high enantioselectivity (up to 82%).

Reductive coupling of aromatic dialkyl acetals using the combination of zinc and chlorotrimethylsilane in the presence of potassium carbonate

The treatment of aromatic acetals with zinc and chlorosilane in the presence of potassium carbonate in toluene brought about facile and effective reductive coupling to give the corresponding coupling products. Copyright

Synthesis and chemistry of enantiomerically pure 10,11-dihydrodibenzo[b,f] thiepines

Several chiral thiepines were efficiently constructed using sulfur diimidazole in combination with a variety of bislithiated carbon fragments. The sulfur atom in these thiepines is found to be unusually unreactive compared to diphenylsulfide. The Royal Society of Chemistry 2006.

"Cation pool" method based on C-C bond dissociation. Effective generation of monocations and dications

The "cation pools" of alkoxyarylcarbenium ions were effectively generated by the oxidative C-C bond dissociation using low temperature electrolysis. The present method is especially effective for the generation and accumulation of dications, which react with carbon nucleophiles. Copyright

Process for the production of chiral compounds

A method for producing chiral compounds according to the condition of a 1.4 Michael reaction, and a compound of formula (31). 1The invention also provides pharmaceutical compositions comprising the compound, and methods for treating pain and other diseases using the pharmaceutical compositions.

Enantioselective catalysis CXXI [1]: Chiral phosphane ligands with additional oxygen functionalities

New optically active phosphane ligands with additional ether and hydroxy functionalities were synthesied and used as sources of enantio-selectivity in the Ni-catalyzed cross coupling reaction of 1-phenylethyl Grignard and vinylbromide and in the Pd-catalyzed allylation of 1,5-dimethylbarbituric acid with allyl acetate.

Design, synthesis, and application of a C2 symmetric chiral ligand for enantioselective conjugate addition of organolithium to α,β-unsaturated aldimine

A C2 symmetric chiral diether ligand, (1R,2R)-1,2-dimethoxy-1,2- diphenylethane, was designed and synthesized on the basis of the concept of an asymmetric oxygen atom. Mediated by the chiral diether, high enantioselectivities were achieved in conjugate addition of organolithiums to naphthaldehyde imine and cyclic and acyclic α,β-unsaturated aldimines. The absolute configuration of the product is predictable by the model.

1,2-Bis-(trialkylsilyl)ethanes: Synthons for vicinal dications?

Anodic oxidation of 1,2-bis-(trimethylsilyl)-1,2-diphenylethane in methanol affords a 65:35 mixture of 1,2-dimethoxy-1,2-diphenylethane (dl:meso = 10:1 and diphenylacetaldehyde dimethylacetal. The results can be interpreted in terms of a 1,2-diaryl-2-methoxyethyl cation, which can undergo either nucleophilic attack by solvent or rearrangement to a 2,2-diaryl-1-methoxyethyl cation. Experiments testing the generality of the reaction are described.