环异构化
对映选择合成
吲哚试验
分子内力
催化作用
化学
药物化学
立体化学
有机化学
作者
Long Huang,Haibin Yang,Di‐Han Zhang,Zhen Zhang,Xiang‐Ying Tang,Qin Xu,Min Shi
标识
DOI:10.1002/anie.201302632
摘要
Bis(indole) alkaloids analogues were prepared under mild conditions and in high yields through a gold-catalyzed cycloisomerization of 1,1-bis(indolyl)-5-alkynes (see scheme). The enantioselective version of this reaction gave the corresponding products in moderate to excellent yields (55–90 %), moderate to good ee values (48–96 %), and satisfactory regioselectivities (3.5:1→20:1).
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