| Literature DB >> 32851781 |
Shuang-Hu Wang1, Rui-Qi Si1, Qing-Bo Zhuang1, Xiang Guo1, Tian Ke2, Xiao-Ming Zhang1, Fu-Min Zhang1, Yong-Qiang Tu1,2.
Abstract
A tandem Bischler-Napieralski/semipinacol rearrangement reaction has been developed for the purpose of assembling a bis(spirocyclic) indole framework, a privileged structural unit of aspidofractinine-type monoterpenoid indole alkaloids, and was used in combination with a subsequent Mannich reaction to expeditiously construct the central bridged bicyclo[2.2.1]heptane ring system of these molecules with contiguous quaternary centers. The development of this novel strategy culminated in the collective total synthesis of four aspidofractinine alkaloids.Entities:
Keywords: Bischler-Napieralski reaction; alkaloids; domino reactions; semipinacol rearrangement; total synthesis
Year: 2020 PMID: 32851781 DOI: 10.1002/anie.202009238
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336