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机构地区:[1]中国药科大学天然药物化学教研室,南京210038
出 处:《中国药科大学学报》2002年第1期73-75,共3页Journal of China Pharmaceutical University
基 金:国家自然科学基金资助项目 ( No.2 9872 0 5 8);高等学校优秀青年教师教学科研奖励计划资助课题
摘 要:AIM To semi-synthesize the similar compounds of (+)-praeruptorin A in order to discover new active compounds. METHODS From natural product Pd-Ib, three similar compounds of (+)-praeruptorin A were obtained purposefully by basic hydrolysis with KOH, reduction with NaBH 4, acylation with acids. RESULTS The structures of synthesized three similar compounds of (+)-Praeruptorin A were 3′( R )-tiglyloxy-4′-keto--3′,4′-dihydroseselin, 3′( S),4′(S ) -diangeloyloxy -3′,4′-dihydroseselin and 3′( S),4′(R )-divaleryloxy-3′,4′-dihydroseselin respectively. CONCLUSION This research work is first semi-synthesis of two known natural product and a new compound from the view of structural modification of (+)-praeruptorin A.AIM To semi-synthesize the similar compounds of (+)-praeruptorin A in order to discover new active compounds. METHODS From natural product Pd-Ib, three similar compounds of (+)-praeruptorin A were obtained purposefully by basic hydrolysis with KOH, reduction with NaBH 4, acylation with acids. RESULTS The structures of synthesized three similar compounds of (+)-Praeruptorin A were 3′( R )-tiglyloxy-4′-keto--3′,4′-dihydroseselin, 3′( S),4′(S ) -diangeloyloxy -3′,4′-dihydroseselin and 3′( S),4′(R )-divaleryloxy-3′,4′-dihydroseselin respectively. CONCLUSION This research work is first semi-synthesis of two known natural product and a new compound from the view of structural modification of (+)-praeruptorin A.
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