60859-79-2

Upstream product

• 20511-20-0 ethyl p-methylcinnamate 
• 626-35-7 nitroacetic acid ethyl ester 
• 2362-77-8 (4-methylbenzylidene)phenylamine 
• 138332-68-0 (Z)-N-phenyl-1-(p-tolyl)methanimine 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 1206899-37-7 C₁₅H₁₈N₂O₆ 
• 1206899-34-4 ethyl 3-(4-methylphenyl)-2-nitro-3-N-(phthalimido)propanoate 
• 1198351-21-1 C₁₆H₁₈N₂O₄ 
• 1255517-09-9 (4S,5R)-3-(ethoxycarbonyl)-5-formyl-5-propyl-4-p-tolyl-4,5-dihydroisoxazole 2-oxide 
• 139927-33-6 ethyl 4-(p-tolyl)-1H-1,2,3-triazole-5-carboxylate 
• 21758-00-9 ethyl 3-(p-tolyl)pent-2-enoate 

Relevant academic research and scientific papers

Catalytic Enantioselective Synthesis of 3,4,5-Trisubstituted Isoxazoline N-Oxides and Regioselective Synthesis of 3,4,5-Trisubstituted Isoxazoles

An efficient catalytic asymmetric synthesis of 3,4,5-trisubstituted isoxazoline N-oxides and regioselective synthesis of 3,4,5-trisubstituted isoxazoles has been described. α-Nitrocinnamates and α-nitrobenzophenones were utilized as Michael acceptors resp

Asymmetric Friedel-Crafts alkylation of indoles with 2-nitro-3-arylacrylates catalyzed by a metal-templated hydrogen bonding catalyst

Abstract An asymmetric Friedel-Crafts alkylation of indoles with 2-nitro-3-arylacrylates catalyzed by a metal-templated hydrogen bonding catalyst has been established. The asymmetric induction relies on chirality transfer solely from the octahedral metal

Nucleophilic addition to nitroacrylates: application towards the synthesis of 2,3-dehydroamino acids and 2,3-diamino acids

The addition of the N-pronucleophiles to 2- or 3-nitro-2-alkenoates in the presence of base provided Michael addition products. In the case of 3-nitro compounds, reaction occurred via the formation of α-adducts and the subsequent elimination of nitrous ac