35583-20-1

Upstream product

• 538-51-2 benzylidene phenylamine 
• 7510-33-0 N,N'-diphenyl-1,2-diphenylethane-1,2-diimine 
• 62-53-3 aniline 
• 134-81-6 benzil 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 100-52-7 benzaldehyde 
• 108-86-1 bromobenzene 
• 29841-69-8 (S,S)-1,2-diphenyl-1,2-diaminoethane 
• 3144-16-9 (1S)-10-camphorsulfonic acid 
• 2879-66-5 rac-1,2-dianilino-1,2-diphenylethane 
• 7439-86-3 2-bromo-1,1,1-trideuterio-ethane 
• 74-96-4 ethyl bromide 

Downstream Products

• 2879-66-5 (+)-N,N'-diphenyl-bibenzyl-α,α'-diyldiamine 
• 135075-62-6 (4RS,5RS)-(E)-3-(1,3,4,5-Tetraphenylimidazolidin-2-yl)propenoate 
• 135075-63-7 (4S,5S)-(-)-(E)-3-(1,3,4,5-Tetraphenylimidazolidin-2-yl)propenoate 
• 135212-30-5 (2R,3R,4R,5S)-5-Phenyl-3-((4S,5S)-1,3,4,5-tetraphenyl-imidazolidin-2-yl)-pyrrolidine-2,4-dicarboxylic acid dimethyl ester 
• 135075-65-9 (2S,3S,4S,5R)-5-Phenyl-3-((4S,5S)-1,3,4,5-tetraphenyl-imidazolidin-2-yl)-pyrrolidine-2,4-dicarboxylic acid dimethyl ester 
• 135075-69-3 (2R,3R,4R,5S)-5-Phenyl-3-((4S,5S)-1,3,4,5-tetraphenyl-imidazolidin-2-yl)-1-(toluene-4-sulfonyl)-pyrrolidine-2,4-dicarboxylic acid dimethyl ester 
• 135075-61-5 (4S,5S)-2-((1S,5R)-6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4,5-tetraphenyl-imidazolidine 
• 135075-66-0 (2S,3S,4S,5R)-5-Phenyl-3-((4S,5S)-1,3,4,5-tetraphenyl-imidazolidin-2-yl)-pyrrolidine-2,4-dicarboxylic acid 2-tert-butyl ester 4-methyl ester 
• 135075-66-0 (2S,3S,4S,5R)-5-Phenyl-3-((4R,5R)-1,3,4,5-tetraphenyl-imidazolidin-2-yl)-pyrrolidine-2,4-dicarboxylic acid 2-tert-butyl ester 4-methyl ester 
• 60644-40-8 (4S,5S)-1,3,4,5-Tetraphenyl-imidazolidine 
• 60644-40-8 1,3-cis-4,5-Tetraphenyl-imidazolidin 

Relevant academic research and scientific papers

New Catalytic Asymmetric Formation of Oxygen Heterocycles Bearing Nucleoside Bases at the Anomeric Carbon

Pyrimidine nucleosides are an important class of compounds with versatile applications across many fields, including biology and medicinal chemistry. Synthesis of nucleoside analogs in optically pure form via traditional glycosylation has always been a ch

Palladium-Catalyzed Asymmetric C(sp3)?H Allylation of 2-Alkylpyridines

The palladium-catalyzed asymmetric side-chain C(α)-allylation of 2-alkylpyridines, without using an external base, was developed. The high linear selectivities and enantioselectivities were achieved using new chiral diamidophosphite monodentate ligands. G

A Metal-Free Approach to 1,2-Diamines via Visible Light-Driven Reductive Coupling of Imines with Perylene as a Photoredox Catalyst

A simple, metal-free, and versatile approach to 1,2-diamines has been developed based on reductive coupling reactions of various imines, where perylene, an aromatic hydrocarbon, was used as a photoredox catalyst under visible light irradiation using a white light-emitting diode. The use of 1 mol % perylene enabled almost complete conversion of the imines, leading to the formation of their corresponding 1,2-diamines, which were isolated in good yields. The ratios between dl and meso diamines ranged from 31:69 to 82:18 depending on the substituents of the imines.

A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis -Vicinal Diamines

A highly stereoselective metal-free hydrogenation of vicinal diimines has been successfully realized for the first time using 5-10 mol % of Piers borane as a catalyst under mild conditions, and a variety of cis-1,2-diamines were obtained in 92-99% yields.

A samarium "soluble" anode: A new source of SmI2 reagent for electrosynthetic application

An electrochemical method to prepare solutions of samarium diiodide in THF is reported. The simple electrolysis of a samarium rod provides a rapid and straightforward in situ synthesis of SmI2. The electrogenerated complex catalyzes various C-C bond formations. The reagent is produced continuously (see scheme) and leads to efficient organic electrosynthesis with significantly smaller amounts of solvent than usually required. Copyright

Homocoupling of aldimines mediated by zirconocene: Synthesis of vicinal diamines and imidazolidines

The reductive coupling of imines in the presence of the lanthanide-originated zirconocene equivalent allows the synthesis of vicinal diamines or imidazolidines under mild conditions in good yields with high diastereoselectivity.

Diastereospecific coupling of imines by low-valent titanium: An experimental and Computational study

The reaction of phenylsilane (PhSiH3) and titanium(IV) isopropoxide [Ti(OiPr)4] generates low-valent titanium alkoxides that reduce and reductively couple imines. The C-C coupling reaction is diastereospecific, with exclusive formati

McMurry coupling of aryl aldehydes and imino pinacol coupling mediated by Ti(O-i-Pr)4/Me3SiCl/Mg reagent

Ti(O-i-Pr)4/Me3SiCl/Mg reagent mediated McMurry coupling of aryl aldehydes to biaryl olefins at near room temperature. This low valent titanium (LVT) reagent also mediated the coupling of aldimines to 1,2-diamines (imino pinacol coupling).

A new Yb3+-catalyzed pinacol and imine-coupling reaction

Ytterbium triflate, Yb(OTf)3, catalyzes the intermolecular reductive homocouplings of imines, aldehydes, and ketones at loadings of 5 mol % in the presence of Mg and Me3SiCl to give isolated yields of up to 95%. Diastereoselectivity of up to 4/96 (dl/meso) is achieved for aromatic aldehydes, up to 100% dl for aliphatic aldehydes, and 100% dl for an intramolecular imine coupling.

Reactivity of the nickel(0)-CO2-imine system: New pathway to vicinal diamines

Nickela-2-oxazolidinones, formed by oxidative coupling of imines and CO2 with Ni0, react with LiCl under mild conditions (4 °C, 1 atm) to afford vicinal diamines in up to 89% yield. The reaction is the first organometallic example of