通过高效的钯-硫脲催化的烷氧基羰基化环化反应实现稠合吡喃γ-内酯的多样性导向合成。
Diversity-oriented synthesis of fused pyran gamma-lactones via an efficient Pd-thiourea-catalyzed alkoxycarbonylative annulation.
作者信息
Li Zhengtao, Gao Yingxiang, Jiao Zhaodong, Wu Na, Wang David Zhigang, Yang Zhen
机构信息
Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University, Shenzhen 518055, China.
出版信息
Org Lett. 2008 Nov 20;10(22):5163-6. doi: 10.1021/ol802115u. Epub 2008 Oct 16.
PMID:18922007
Abstract
We reported herein a diversity-oriented synthesis of a range of fused pyran-gamma-lactones that was effected through a versatile Pd-thiourea complex-catalyzed intramolecular alkoxycarbonylative annulation.
摘要
我们在此报道了一系列稠合吡喃-γ-内酯的多样性导向合成，该合成通过一种通用的钯-硫脲配合物催化的分子内烷氧羰基化环化反应实现。
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