1396203-86-3

Upstream product

• 1396201-44-7 5-hydroxy-1-(3,4-dimethoxyphenyl)pentan-1-one 
• 1396202-52-0 ethyl 7-(3,4-dimethoxyphenyl)-7-oxohept-2-enoate 
• 67-63-0 isopropyl alcohol 
• 2859-78-1 4-Bromoveratrole 
• 1396201-89-0 5-(3,4-dimethoxyphenyl)-5-oxopentanal 

Relevant academic research and scientific papers

Enantioselective synthesis of 2,6-cis-disubstituted tetrahydropyrans via a tandem catalytic asymmetric hydrogenation/oxa-Michael cyclization: An efficient approach to (-)-centrolobine

A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and oxa-Michael cyclization for the synthesis of 2,6-cis-disubstituted tetrahydropyrans has been developed (ee up to 99.9%, cis/trans-selectivity up to 99:1). T