First total synthesis of the marine illudalane sesquiterpenoid alcyopterosin EElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b2/b209573d/
作者:Bernhard Witulski、Axel Zimmermann、Nicholas D. Gowans
DOI:10.1039/b209573d
日期:2002.11.29
The first synthesis of the marine illudalane sesquiterpenoid alcyopterosin E was accomplished through a concise ABC ring-formation strategy using a rhodium(I)-catalysed intramolecular alkyne cyclotrimerisation as key connection.
通过使用铑(I)催化的分子内炔烃环三聚体作为关键连接的简洁的ABC环形成策略,实现了海洋伊卢达烷倍半萜烯类环蝶呤E的首次合成。