1437872-98-4

Upstream product

• 5274-70-4 3-nitrosalicylic aldehyde 
• 1446418-41-2 methyl 2-(allyloxy)-3-nitrobenzoate 
• 22621-41-6 2-hydroxy-3-nitro-benzoic acid methyl ester 

Downstream Products

• 1437872-81-5 methyl 3-(3-(2-(allyloxy)-3-nitrobenzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-75-7 methyl 3-(3-(2-hydroxy-3-(2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-83-7 methyl 3-(3-(2-(allyloxy)-3-(2-methoxy-3-(2-methoxy-3-nitrobenzamido)benzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 
• 1437872-82-6 methyl 3-(3-(2-(allyloxy)-3-(2-methoxy-3-nitrobenzamido)benzamido)-2-methoxybenzamido)-2-methoxybenzoate 

Relevant academic research and scientific papers

Organoselenium and DMAP co-catalysis: Regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes

A catalytic system consisting of bis(4-methoxyphenyl)selenide and 4-(dimethylamino)pyridine (DMAP) has been developed for the regioselective synthesis of medium-sized bromo/iodo lactones and bromooxepanes possessing high transannular strain. 77Se NMR, mass spectrometry and theoretical studies reveal that the reaction proceeds via a quaternary selenium intermediate.

Patterned recognition of amines and ammonium ions by a stimuli-responsive foldamer-based hexameric oligophenol host

A stimuli-responsive hexameric oligophenol host undergoes amine-induced co-operative folding from a more fluorescent, more linear structure into less fluorescent, more curved or helically folded states, enabling easy identification and classification of the bound amine guests. The Royal Society of Chemistry 2013.