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Spectral Data of Chemical Modification Products of Costunolide
Authors:Tiansheng Lu  Nikolaus H Fischer
Institution:Department of Chemistry , Louisiana State University , Baton Rouge , Louisiana , 70803 , U. S. A.
Abstract:Epoxidation of costunolide (1) yielded parthenolide (3), 1, 10-epoxycostunolide (4), and the cyclization products of 4, santamarin (5), reynosin (6), magnolialide (7) and a 1, 4-epoxyeudesmanolide (8). Reduction of santamarin (5) with sodium borohydride afforded 11, 13-dihydrosantamarin (9) and an eudesmen-triol (10). Reduction of reynosin (6) provided 11, 13-dihydroreynosin (11) and the two eudesman-triols 12 and 13. The structures of the new compounds were elucidated by ID and 2D 1H and 13C NMR spectral methods.
Keywords:Sesquiterpene lactones  germacranolides  costunolide  epoxidation-cyclization  parthenolide  1  10-epoxycostunolide  eudesmanolides  reductions  1H and 13C NMR  
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