102368-34-3

Upstream product

• 14224-99-8 2-methyl-4,5-diphenyloxazole 
• 4675-18-7 4,5-diphenyloxazole 
• 68-12-2 N,N-dimethyl-formamide 
• 51891-89-5 2-oxo-1,2-diphenylethyl-2-chloroacetate 
• 101273-85-2 4,5-diphenyloxazol-2-yl-methanol 

Downstream Products

• 102368-33-2 (E)-3-methyl-4-(4,5-diphenyloxazol-2-yl)but-3-en-2-one 
• 917988-94-4 (E)-3-(4,5-diphenyloxazol-2-yl)acrylaldehyde 
• 102368-39-8 2,3-dimethyl-3-hydroxy-4-<(methoxymethyl)oxy>-1-(4,5-diphenyloxazol-2-yl)-1,4,5-hexatriene 
• 102368-42-3 4-(4,5-Diphenyl-oxazol-2-yl)-2,3-dimethyl-5-methylene-cyclopent-2-enone 
• 124771-33-1 (E)-2-isopropyl-3-methyl-3-hydroxy-4-<(methoxymethyl)oxy>-1-(4,5-diphenyloxazol-2-yl)-1,4,5-hexatriene 
• 102368-43-4 4-(4,5-Diphenyl-oxazol-2-yl)-3-isopropyl-2-methyl-5-methylene-cyclopent-2-enone 
• 929882-98-4 (2R,3R)-S-ethyl 5-(4,5-diphenyloxazol-2-yl)-2-methyl-3-(triethylsilyloxy)pentanethioate 
• 1026559-05-6 C₇₃H₁₂₉NO₉Si₆ 
• 917988-95-5 (S)-4-benzyl-3-((2R,3R,E)-5-(4,5-diphenyloxazol-2-yl)-3-hydroxy-2-methylpent-4-enoyl)oxazolidin-2-one 
• 917988-96-6 (S)-4-benzyl-3-((2R,3R)-5-(4,5-diphenyloxazol-2-yl)-3-hydroxy-2-methylpentanoyl)oxazolidin-2-one 
• 102368-35-4 (E)-3-isopropyl-4-(4,5-diphenyloxazol-2-yl)but-3-en-2-one 
• 102368-36-5 (Z)-3-isopropyl-4-(4,5-diphenyloxazol-2-yl)but-3-en-2-one 

Relevant academic research and scientific papers

Photoinduced Intramolecular formal [4 + 2] Cycloaddition of Aryl-Substituted o-Vinylstyryl-2-oxazoles to Form Benzo[f]quinoline Derivatives: Experimental Results and Theoretical Interpretation

A new approach to benzo[f]quinoline derivatives has been found by an effective formal [4 + 2] photocycloaddition process from novel aryl-substituted o-vinylstyryl-2-oxazoles. All of the o-vinylstyryl-2-oxazoles were synthesized by a multicomponent Wittig

Oxazoles for click chemistry II: Synthesis of extended heterocyclic scaffolds

Abstract New routes to 2,4,5-trisubstituted oxazoles were established whereby the substitution pattern was established by the structure of the starting nonsymmetrical acyloins. 2-Chloromethyl-4, 5-disubstituted oxazoles were prepared by refinements of an earlier described process whereby chloroacetyl esters of symmetrical and nonsymmetrical acyloins were cyclized using an ammonium acetate/acetic acid protocol. After substitution is effected, the azide moiety is then installed by substitution under mild conditions. While dibrominated and iodinated phenyloxazoles are required for further synthetic elaboration, the cyclization reaction was found to be very sensitive to the relative positions of the halogens in the starting materials.

Enantioselective synthesis of oasomycin A, part II: Synthesis of the C29-C46 subunit

(Chemical Equation Presented) Putting the pieces together: The total synthesis of the natural macrolide oasomycin A has been realized. Key fragment couplings include an anti-Felkin selective aldol addition (green), Kociensky-Julia olefinations (red), and

Methods of using heterocycle-amine ligands, compositions, complexes, and catalysts

Ligands, compositions, and metal-ligand complexes that incorporate heterocycle-amine compounds are disclosed that are useful in the catalysis of transformations such as the polymerization of monomers into polymers. The catalysts have high performance characteristics, including higher comonomer incorporation into ethylene/olefin copolymers, where such olefins are for example, 1-octene, propylene or styrene. The catalysts also polymerize propylene to form isotactic polypropylene.