Catalytic Enantioselective Steglich-Type Rearrangement of Enol Lactones: Asymmetric Synthesis of Spirocyclic 1,3-Diketones

Autor: Xiao-Yan Zhang, Ka Lu, Bao-Kuan Guo, Ya-Ping Shao, Hong Wang, Fu-Min Zhang, Yong-Qiang Tu, Xiao-Ming Zhang
Rok vydání: 2022
Předmět:
Zdroj: The Journal of organic chemistry. 87(22)
ISSN: 1520-6904
Popis: An example of asymmetric Steglich-type rearrangement of enol lactones is reported. This highly enantioselective acyl transfer reaction is catalyzed by chiral isothiourea at ambient temperature and provides a useful synthetic approach to access enantioenriched spirotricyclic β,β'-diketones from a broad range of indanone or tetralone-derived lactones. Preliminary mechanistic studies suggest the initial formation of an
Databáze: OpenAIRE