期刊
TETRAHEDRON
卷 63, 期 26, 页码 5903-5917出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2007.02.021
关键词
sesquiterpenoid; Celastraceae; polyhydroxylation; epoxidation; insecticide
A concise and efficient synthesis of the C-13 tricyclic core of the dihydro-beta-agarofuran skeleton common to the natural Celastraceae sesquiterpenoids is described. The strategy entails a Mukaiyama aldol reaction of a tetrahydronaphthalene enol silane with acetone, epoxidation, ketone reduction, and acid-catalyzed cyclization. This key scaffold was converted into diverse polyhydroxylated derivatives, which were tested for insecticidal activity. (C) 2007 Elsevier Ltd. All rights reserved.
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