863555-48-0

Upstream product

• 74181-34-3 2,2,-dimethyl-1,3-dioxan-5-one 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 863555-54-8 (-)-(1R,2S,4S,7R)-7-benzyloxymethyl-2-formylbicyclo[2.2.1]hept-5-en-2-yl p-methoxybenzoate 
• 863555-53-7 (-)-(1S,2S,4S)-2-formylbicyclo[2.2.1]hept-5-en-2-yl p-methoxybenzoate 
• 863555-49-1 α-(p-methoxybenzoyloxy)acrolein 

Relevant academic research and scientific papers

Design of an organocatalyst for the enantioselective Diels-Alder reaction with α-acyloxyacroleins

We have realized the first enantioselective organocatalytic Diels-Alder reaction between α-substituted acroleins, such as α-acyloxyacroleins, and not only cyclic but also acyclic dienes. α-Acyloxyacroleins are useful as synthetic equivalents of α-haloacro

Chiral 1,1′-binaphthyl-2,2′-diammonium salt catalysts for the enantioselective Diels-Alder reaction with α-acyloxyacroleins

A diammonium salt of chiral 1,1′-binaphthyl-2,2′-diamine and trifluoromethanesulfonimide (Tf2NH) shows excellent catalytic activity and enantioselectivity for the Diels-Alder reaction of α-acyloxyacroleins with cyclic dienes. For example, in th