Synthetic studies on prehispanolone and 14,15-dihydroprehispanolone
Publication in refereed journal


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摘要Employing an intramolecular Michael addition as a pivotal step, butenolide 5, furans 6 and 7 have been converted to dioxaspiro compounds 8, 9, 10 and Il,whose heterocyclic frameworks constitute important structural units of prehispanolone (2) as well as 14,15-dihydroprehispanolones (3) and (4), respectively. Hispanolone (1) was converted to 2, 3 and 4 by utilizing a similar strategy. Copyright (C) 1996 Elsevier Science Ltd
著者Wang ES, Choy YM, Wong HNC
期刊名稱Tetrahedron
出版年份1996
月份9
日期9
卷號52
期次37
出版社PERGAMON-ELSEVIER SCIENCE LTD
頁次12137 - 12158
國際標準期刊號0040-4020
語言英式英語
Web of Science 學科類別Chemistry; Chemistry, Organic; CHEMISTRY, ORGANIC

上次更新時間 2020-06-08 於 02:05