化学
十一烷
立体中心
分子内力
羟醛反应
羟醛缩合
全合成
立体化学
组合化学
甲磺酸
三环
对映选择合成
有机化学
催化作用
作者
Jian Xiao,Zi-Hao Liu,Zhiying He,Ping Wu,Ya‐Wen Wang,Wei‐Dong Z. Li,Yu Peng
标识
DOI:10.1021/acs.orglett.4c02877
摘要
A bioinspired total synthesis of 3-epi-junipercedrol, which contains a strained tricyclo[5.2.2.03,7]undecane allo-cedrane framework and five stereocenters, was accomplished via an effective anionic semipinacol rearrangement of a tricyclic cedrane mesylate. The corresponding cedrane precursor was synthesized efficiently by employing the reductive oxy-Nazarov cyclization and an intramolecular aldol condensation as the key steps. This synthetic approach provided a further evidence for the biogenetic relationship between the typical cedrane and allo-cedrane sesquiterpenoids.
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