848645-69-2

Upstream product

• 20781-20-8 2,4-Dimethoxybenzylamine 
• 848645-68-1 1-(2,4-dimethoxybenzyl)aziridine-2-carboxylic acid ethyl ester 

Downstream Products

• 848645-61-4 1-(2,4-dimethoxybenzyl)-2-vinylaziridine 
• 848645-60-3 (R)-(+)-1,3-bis(2,4-dimethoxybenzyl)-4-vinylimidazolidin-2-one 
• 848645-70-5 (R)-(-)-1,3-bis(2,4-dimethoxybenzyl)-4-vinylimidazolidine 
• 848645-71-6 (R)-(-)-N',N''-bis(2,4-dimethoxybenzyl)but-3-ene-1,2-diamine 

Relevant academic research and scientific papers

Metal-free aza-Claisen type ring expansion of vinyl aziridines: An expeditious synthesis of seven membered N-heterocycles

A metal-free approach for the synthesis of 7-membered aza-heterocycles has been developed by the intermolecular [5 + 2] cycloaddition of non-activated vinylaziridines and alkynes. This method has a broad substrate scope under mild reaction conditions to a

DYKAT of vinyl aziridines: Total synthesis of (+)-pseudodistomin D

(Chemical Equation Presented) A concise total synthesis of (+)-pseudodistomin D was developed. The absolute stereochemistry was established through a dynamic kinetic asymmetric cycloaddition of an isocyanate to a vinyl aziridine. The piperidine core was c