24513-01-7

Upstream product

• 24393-54-2 ethyl 3-(2-methoxyphenyl)prop-2-enoate 
• 637-81-0 ethyl-2-azidoacetate 
• 135-02-4 ortho-anisaldehyde 

Downstream Products

• 129801-34-9 C₃₀H₂₈NO₃P 
• 100-52-7 benzaldehyde 
• 43142-25-2 ethyl 4-methoxy-indole-2-carboxylate 
• 129801-48-5 5-Methoxy-1-((4-methoxy-phenyl)-{1-(4-methoxy-phenyl)-4-[1-(2-methoxy-phenyl)-meth-(E)-ylidene]-5-oxo-4,5-dihydro-1H-imidazol-2-yl}-amino)-isoquinoline-3-carboxylic acid ethyl ester 
• 129801-47-4 5-Methoxy-1-({4-[1-(2-methoxy-phenyl)-meth-(E)-ylidene]-5-oxo-1-p-tolyl-4,5-dihydro-1H-imidazol-2-yl}-p-tolyl-amino)-isoquinoline-3-carboxylic acid ethyl ester 
• 129801-39-4 1-(4-Chloro-phenylamino)-5-methoxy-isoquinoline-3-carboxylic acid ethyl ester 
• 129801-43-0 (Z)-3-(2-Methoxy-phenyl)-2-(4-methoxy-phenyliminomethyleneamino)-acrylic acid ethyl ester 
• 129801-44-1 (Z)-2-(4-Chloro-phenyliminomethyleneamino)-3-(2-methoxy-phenyl)-acrylic acid ethyl ester 
• 129801-42-9 (Z)-3-(2-Methoxy-phenyl)-2-p-tolyliminomethyleneamino-acrylic acid ethyl ester 
• 129801-50-9 4-[1-(2-Methoxy-phenyl)-meth-(Z)-ylidene]-2-p-tolyl-4H-oxazol-5-one 

Relevant academic research and scientific papers

Visible-Light-Mediated Synthesis of Pyrazines from Vinyl Azides Utilizing a Photocascade Process

A convenient method for the synthesis of substituted pyrazines from vinyl azides has been developed. This method is enabled by a dual-energy and electron-transfer strategy by visible-light photocatalysis. Initially, vinyl azides are activated by a triplet sensitization process from an excited ruthenium photocatalyst in the presence of water to form dihydropyrazines, followed by a single-electron-transfer (SET) process under oxygen (air) atmosphere that leads to the tetrasubstituted pyrazines in good to excellent yields.

Tripeptidylpeptidase inhibitors

A compound of formula wherein the substituents are defined as in the specification and salts or hydrates thereof is disclosed as well as a method of treating disorders associated with the inactivation or excessive degradation of cholecystokinin.

A novel synthesis of α-azidocinnamates, α-azido-α,β-unsaturated ketones and β-azidostyrenes mediated by cerium(IV) ammonium nitrate

Cerium(IV) ammonium nitrate mediated addition of azide to cinnamic esters, acids and α,β-unsaturated ketones, followed by reaction with sodium acetate afforded the α-azidocinnamates, β-azidostyrenes and α-azido-α,β- unsaturated ketones, respectively, in good yields. (C) 2000 Elsevier Science Ltd.

Preparation and Thermal Ring-closure of β-Aryl Vinyl Carbodi-imides: Synthesis of Isoquinoline Derivatives

Reaction of the iminophosphoranes (7)-(9), derived from α-azidocinnamates and triphenylphosphine, with aromatic isocyanates gives either 1-arylaminoisoquinoline-3-carboxylates (10)-(12) or the corresponding carbodi-imides (14)-(18) which by thermal treatm