31143-28-9

Upstream product

• 186581-53-3 diazomethane 
• 34620-73-0 ent-Fisetinidol-4β-ol 
• 6515-24-8 (+/-)-2,3-trans-3-hydroxy-3',4',7-trimethoxyflavan 
• 490-32-4 (+/-)-2r-(3,4-Dihydroxy-phenyl)-chroman-3t,4c,7-triol 
• 1166-04-7 3',4',7'-tri-O-methylfisetinidol-4α-ol 
• 490-32-4 (-)-luecofisetinidin 

Downstream Products

• 20772-32-1 (2S)-3t,4c-Diacetoxy-2r-(3,4-dimethoxy-phenyl)-7-methoxy-chroman 
• 1166-04-7 (+/-)-mollisacacidin 7,3',4'-trimethyl ether 
• 88038-03-3 (3aS)-4c-(3,4-dimethoxy-phenyl)-7-methoxy-2,2-dimethyl-(3ar,9bc)-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromene 
• 96582-13-7 (+/-)-3t,4t-Bis-benzoyloxy-2r-(3,4-dimethoxy-phenyl)-7-methoxy-chroman 
• 4283-55-0 (2rH)-3c,4t-Diacetoxy-7,3',4'-trimethoxy-flavan 
• 88038-03-3 (+/-)-4c-(3,4-dimethoxy-phenyl)-7-methoxy-2,2-dimethyl-(3ar,9bc)-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromene 
• 4283-55-0 Acetic acid (2R,3R,4R)-4-acetoxy-2-(3,4-dimethoxy-phenyl)-7-methoxy-chroman-3-yl ester 
• 105072-75-1 (2R,3S)-2,3-trans-3-acetoxy-6-<(2S,3R,4S)-2,3-trans-3,4-cis-3-acetoxy-3',4',7-trimethoxyflavan-4-yl>-8-<(2S,3R,4R)-2,3-trans-3,4-trans-3-acetoxy-6,8-bi-<(2S,3R,4R)-2,3-trans-3,4-trans-3-acetoxy-3',4',7-trimethoxyflavan-4-yl>-3',4',7-trimethoxyflavan...> 

Relevant academic research and scientific papers

HETEROCYCLES. XVIII. SYNTHESIS OF THE RACEMATES OF NATURALLY OCCURRING FLAVONOIDS

Racemic aromadendrin and fustin have been stereoselectively synthesized.Reduction of the O-substituted derivatives of these flavanonols provides the corresponding derivatives of gleditsin, leucopelargonidin and mollisacacidin (leucofisetinidin).

Synthesis of Condensed Tannins. Part 11. Intramolecular Enantiomerism of the Constituent Units of Tannins from the Anacardiaceae: Stoicheiometric Control in Direct Synthesis: Derivation of 1H Nuclear Magnetic Resonance Parameters Applicable to

Tannins from the heartwoods of Schinopsis spp. (quebracho) and Rhus spp.(karee) represent mutual condensation products of their associated precursors (2S,3R,4S)(-)-leucofisetinidin, (2R,3S)-(+)-catechin and, to a minor extent, (2R,3R)-(-)-epicatechin.The