31367-42-7

Upstream product

• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 83739-61-1 1-(2-bromo-1-methoxyethyl)-4-methoxybenzene 
• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 67-56-1 methanol 
• 637-69-4 4-Methoxystyrene 
• 17508-17-7 O-(2,4-dinitrophenyl)hydroxylamine 
• 123-11-5 4-methoxy-benzaldehyde 
• 31367-41-6 1-methoxy-4-(1-methoxy-2-nitro-ethyl)-benzene 

Downstream Products

• 70546-93-9 N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide 
• 245732-46-1 2-(p-methoxyphenyl)-2-methoxyethyldithiocarbamate 

Relevant academic research and scientific papers

DIRECT STEREOSPECIFIC SYNTHESIS OF UNPROTECTED AZIRIDINES FROM OLEFINS

A method for the direct stereospecific conversion of structurally diverse mono-, di-, tri- and tetra-substituted olefins to N-H, N-alkyl, N-cycloalkyl, or N-aralkyl aziridines using a hydroxylamine amination agent with transition metal catalyst. The method is operationally simple (i.e., one-pot), scalable and fast at ambient temperature.

Synthetic studies of the tridentatols

(Matrix presented) The tridentatols are conjugated tyramine derivatives isolated from the Atlantic hydroid Tridentata marginata and have potentially useful properties in sunscreen applications. Preparations of tridentatol C and two tridentatol A analogues