📜高香草酸置于三氟化硼乙醚,甲基磺酰氯体系中,用 N,N-二甲基甲酰胺 用作溶剂,化学反应 2.5H,反应生成7,4'-二羟基-3'-甲氧基异黄酮 参考文献:Waehaelae,Kristiina; Hase,Tapio A.,Journal Of The Chemical Society. Perkin Transactions I,1991,# 12,P. 3005-3008 标题:Waehaelae,Kristiina; Hase,Tapio A.,Journal Of The Chemical Society. Perkin Transactions I,1991,# 12,P. 3005-3008
参考标题:Synthesis Of Various Kinds Of Isoflavones, Isoflavanes, And Biphenyl-Ketones And Their 1,1-Diphenyl-2-Picrylhydrazyl Radical-Scavenging Activities 作者:Hideyuki Goto,Yoshiyasu Terao,Shuji Akai 摘要:Forty-Eight Kinds Of Isoflavones (8), Thirty-One Isoflavanes (9), And Forty-Seven Biphenyl-Ketones (10, 10′) Were Synthesized From Eleven Kinds Of Substituted Phenols (11) And Six Phenylacetic Acids (12). Among Them, Seventy-Five Compounds Are New. The Radical Scavenging Activities Of These Compounds Were Evaluated Using 1,1-Diphenyl-2-Picrylhydrazyl (Dpph) At Ph 6.0. We Found That Thirty-Nine Out Of Forty-Three Compounds Having A Catechol Moiety On Either The A- Or The B-Ring Exhibited A High Activity (Ed50=12-54 μm) Similar To That Of Catechin. In These Cases, The Remaining Part Of Their Structure Seemed To Have Little Effect On Their Activity. Many 6- Or 8-Hydroxyisoflavanes (9E-I) And Their Biphenyl-Ketone Derivatives (10E-H) Also Showed A High Activity (Ed50=<50 μm), While All Of Their Corresponding Isoflavones (8E-I) Were Not Active At All. The 7-Hydroxyisoflavanes Having Either An Additional Hydroxyl Group At The C5-Position (9D) Or A Methoxy Group At The C6-Position (9J) Presented A High Activity (Ed50=26-32 μm). This Study Suggests That Natural Isoflavones Have The Possibilities Of Exhibiting Antioxidant Activities Through The Hydroxylation At The C6-, C8-, Or C3′-Position Or The Formation Of The Isoflavanes (9) And/or The Biphenyl-Ketone Derivatives (10′) By Metabolism Or Biotransformation.
合成参考文献
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