42956-08-1

Upstream product

• 98-80-6 phenylboronic acid 
• 100-52-7 benzaldehyde 
• 75-31-0 isopropylamine 
• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 88782-86-9 (+/-)-Isopropyl-<1,3-diphenyl-prop-2-enyl>-amin 
• 148920-79-0 Ru(CO)2(P(C₆H₅)3)(C₆H₅CHCHCHNCH(CH₃)2) 
• 201554-84-9 pentacarbonyl[2-ethoxy-1-isopropyl-4,5-diphenyl-1-azonia-5H-cycloheptatriene-3-yl]tungstate 
• 201554-83-8 3-(2-ethoxy-1,1,1,1,1-pentacarbonyl-1-tungsta-2-ethenyl)-1-isopropyl-2,4-diphenyl-1,4-dihydro-pyridine 
• 201554-89-4 pentacarbonyl[2-ethoxy-1-isopropyl-4,5-diphenyl-1-azonia-5H-cycloheptatriene-3-yl]chromate 
• 201554-88-3 3-(2-ethoxy-1,1,1,1,1-pentacarbonyl-1-chroma-2-ethenyl)-1-isopropyl-2,4-diphenyl-1,4-dihydro-pyridine 
• 93144-86-6 (+/-)-<1-Butyl-3-phenyl-prop-2-enyl>-isopropyl-amin 
• 1392216-43-1 7,8-dihydro-1-isopropyl-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H)-one 
• 174090-39-2 Cr(CO)5(C₆H₅)2(CH₃)3OCH₂(C₆H₂N) 

Relevant academic research and scientific papers

Silylative Reductive Amination of α,β-Unsaturated Aldehydes: A Convenient Synthetic Route to β-Silylated Secondary Amines

Described here is a reductive amination/hydrosilylation cascade of α,β-unsaturated aldehydes mediated by a Lewis acidic borane catalyst. The present reaction system provides an one-pot synthetic route towards β-silylated secondary amines that have not been accessible by other previous catalysis. Comparative 1H NMR studies on the silylative reduction of enimines revealed that steric bulkiness of primary amine reactants strongly affects both catalytic efficiency and regioselectivity. This strategy was applicable to a broad range of substrates and amenable to one-pot gram-scale synthesis. Moreover, a diastereoselective introduction of the β-silyl group was also found to be feasible (d.r. up to 71:29).

Modular access to vicinally functionalized allylic (thio)morpholinonates and piperidinonates by substrate-controlled annulation of 1,3-azadienes with hexacyclic anhydrides

A modular substrate-controlled hexannulation of inherently promiscuous 1,3-azadienes with hexacyclic anhydrides, which affords versatile vicinally functionalized allylic lactams, in high yields, regio- and stereoselectivities is described.

Efficient synthesis of N-Substituted 4-arylquinoline derivatives using ZnCl2 or ZrO2

N-Substituted 7,8-dihydro-7,7-dimethyl-4-arylquinolin-5(1H,4H,6H)-ones 4a-l have been reported by one-pot reaction of cinnamaldehyde derivatives, dimedone and various amines in the presence of ZnCl2 or ZrO2 in fairly high yields.

A simple and inexpensive method for the preparation of imines and azadienes

A number of imines and azadienes were prepared in high yield and good purity by using the condensation reactions of various aldehydes and ketones with amines over natural Algerian bentonite.

Organometallic Reactions of Conjugated Azomethines, IV. Catalytic Synthesis of Substituted Cyclohexanes from Butadiene and 1-Azadienes with ?-Allyl Palladium Complexes

The reaction of dimeric ?-allyl palladium chloride with 1-azadienes 1 (R-N=CH-CH=CH-R') affords the mononuclear complexes (?-Allyl)Pd(L)Cl 2.Two independent intramolecular rotational motions are detected by NMR methods.These complexes (with R' = Aryl) rea

Halogenated Ketenes. 38. Cycloaddition of α,β-Unsaturated Imines with Ketenes To Yield Both β- and δ-Lactams

The cycloaddition of various types of α,β-unsaturated imines with diphenyl- and dichloroketenes yields both (2 + 2) and (4 + 2) cycloaddition products, i. e., β-lactams and δ-lactams, respectively.The cycloaddition products are dependent upon substitution in the imine and the ketene.The δ-lactams derived from dichloroketene are easily dehydrochlorinated to the corresponding 2-pyridones.All of the results are consistent with a two-step cycloaddition process involving a dipolar intermediate.