55568-95-1

Upstream product

• 1621-55-2 rac-trans-3-hydroxy-2-phenyl-3,4-dihydro-2H-chromen-4-one 
• 40524-63-8 2'-O-methoxymethylchalcone 
• 95280-66-3 2,3-epoxy-1-2'-methoxymethoxyphenyl-3-phenylpropanone 
• 1621-55-2 Flavanon-3-ol 
• 91299-68-2 2,3-epoxy-1-2'-methoxymethoxyphenyl-3-phenylpropanol 
• 888-12-0 (E)-2'-hydroxy-chalcone 
• 24114-57-6 3-(2-hydroxyphenyl)-1-phenyl-1-propene 
• 118-93-4 o-hydroxyacetophenone 
• 100-52-7 benzaldehyde 
• 1214-47-7 1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one 

Downstream Products

• 20754-85-2 C₂₉H₂₂O₅ 
• 20754-85-2 C₂₉H₂₂O₅ 
• 103165-66-8 (+/-)-3t,4c-Bis-(4-nitro-benzoyloxy)-2r-phenyl-chroman 
• 1032-31-1 (+/-)-4c-phenyl-(3ar,9bc)-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromen-2-one 
• 1036-02-8 (+/-)-2,2-dimethyl-4c-phenyl-(3ar,9bc)-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromene 

Relevant academic research and scientific papers

Enantioselective selenocyclization via dynamic kinetic resolution of seleniranium ions by hydrogen-bond donor catalysts

Highly enantioselective selenocyclization reactions are promoted by the combination of a new chiral squaramide catalyst, a mineral acid, and an achiral Lewis base. Mechanistic studies reveal that the enantioselectivity originates from the dynamic kinetic resolution of seleniranium ions through anion-binding catalysis.

Heterocycles. XV. Enantioselective Synthesis of Chiral Flavanonols and Flavan-3,4-diols

Chiral flavanonols and flavan-3,4-diols have been enantioselectively synthesized from the chiral epoxychalcones (-)-2a and (+)-2b, which are obtained by the asymmetric epoxidation of the chalcone 1 under phase-transfer conditions.The absolute configuratio

HETEROCYCLES. XIV. EFFICIENT STEREOCONTROLLED SYNTHESIS OF RACEMIC FLAVONOIDS

Stereocontrolled synthesis of the flavonoids (2, 4 and 5) is described.Racemic taxifolin (dihydroquercetin) (14) is synthesized by application of this method.