134733-96-3

Upstream product

• 110-00-9 furan 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 135007-81-7 <6-acetoxy-3-amino-2-(3,4-dimethoxyphenyl)tetrahydro-2H-pyran-3-yl>methylamine dihydrochloride 
• 135007-79-3 2-<1,5-dihydro-1-(3,4-dimethoxyphenyl)>pentanamine hydrochloride 
• 134734-09-1 <6-acetoxy-3-N-benzylamino-2-(3,4-dimethoxyphenyl)tetrahydro-2H-pyran-3-yl>carbonitrile 
• 134734-10-4 N-<2-acetoxy-6-(3,4-dimethoxyphenyl)tetrahydro-2H-pyran-5-yl>acetamide 
• 134734-03-5 6-acetoxy-2-(3,4-dimethoxyphenyl)-3-hydroxyiminotetrahydro-2H-pyran-3-one 
• 134734-01-3 6-acetoxy-2-(3,4-dimethoxyphenyl)-tetrahydro-2H-pyran-3-one 
• 134734-15-9 <6-acetoxy-2-(3,4-dimethoxyphenyl)tetrahydro-2H-pyran-3-yl>amine 
• 134733-99-6 6-acetoxy-2-(3,4-dimethoxyphenyl)-2H-pyran-3(6H)-one 
• 134734-11-5 N-<6-(3,4-dimethoxyphenyl)-2-hydroxytetrahydro-2H-pyran-5-yl>acetamide 
• 134734-12-6 5-acetylamino-6-(3,4-dimethoxyphenyl)-δ-valerolactone 
• 134734-05-7 2-(3,4-dimethoxyphenyl)-6-hydroxy-3-hydroxyiminotetrahydro-2H-pyran-3-one 
• 134734-07-9 1-(3,4-dimethoxyphenyl)-2-hydroxyimino-1,5-pentanodiol 
• 134733-97-4 2-(3,4-dimethoxyphenyl)-6-hydroxy-2H-pyran-3(6H)-one 

Relevant academic research and scientific papers

Catalytic Enantioselective Aza-Piancatelli Rearrangement

An efficient organocatalytic enantioselective aza-Piancatelli rearrangement is disclosed. The powerful process provides rapid access to valuable chiral 4-amino-2-cyclopentenone building blocks from readily available 2-furfurylcarbinols with excellent chemo-, enantio-, and diastereoselectivities under mild reaction conditions.