Synthetic Studies toward Lindenane-type Dimers via Diels-Alder Reaction
Publication in refereed journal

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其它資訊
摘要Lindenane-type dimers are natural sesquiterpenoids, mainly from Chloranthaceae, possessing an unique heptacyclic skeleton and diverse bioactivities. Inspection of their structures suggested the possibility of deploying an endo Diels-Alder reaction to construct the key cyclohexene ring. In this article we investigated the feasibility of Diels-Alder reactions between various dienes and dienophiles, leading ultimately to their applications to the realization of [4 + 2] lindenane dimers.
出版社接受日期05.10.2018
著者Jian-Li Wu, Yin-Suo Lu, Henry N.C. Wong, Xiao-Shui Peng
期刊名稱Tetrahedron
出版年份2018
月份11
日期22
卷號74
期次47
出版社Elsevier Ltd.
出版地Amsterdam
頁次6749 - 6760
國際標準期刊號0040-4020
語言美式英語
關鍵詞Diels-Alder, Lindenane, Sesquiterpenoid, Total synthesis

上次更新時間 2020-21-10 於 02:21