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作 者:朱燕云[1] 陈希慧[1] 黄初升[2] 刘红星[2] 凌新龙[2]
机构地区:[1]广西大学化学化工学院,南宁530004 [2]广西师范学院应用化学研究所,南宁530001
出 处:《应用化学》2005年第5期560-562,共3页Chinese Journal of Applied Chemistry
基 金:国家自然科学基金(20062001);广西自然科学基金(0007016);广西"新世纪十百千人才工程"资金(20012205)资助项目
摘 要:A concise route for the total syntheses of benzopranylchalcones from 2,4,6-trihydroxyacetophone(3) and citral(8), by means of cyclization, methoxy-protection and aldol-condensation is described. Two benzopranylchalcones, Boesenbergin B(1) and Boesenbergin A(2) were synthesized from 2,4,6-(trihydroxyacetophone)(3), citral(8) and benzaldehyde(9) via the route. The total yields of compounds 1 and 2 were 26% and 11%, respectively. In the cyclization step, the yields of key intermediates 4 and 7 were 40% and 42%, respectively.A concise route for the total syntheses of benzopranylchalcones from 2,4,6-trihydroxyacetophone(3) and citral(8), by means of cyclization, methoxy-protection and aldol-condensation is described. Two benzopranylchalcones, Boesenbergin B(1) and Boesenbergin A(2) were synthesized from 2,4,6-(trihydroxyacetophone)(3), citral(8) and benzaldehyde(9) via the route. The total yields of compounds 1 and 2 were 26% and 11%, respectively. In the cyclization step, the yields of key intermediates 4 and 7 were 40% and 42%, respectively.
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