| Literature DB >> 26138939 |
Shifa Zhu1, Qiaohui Zhang2, Kai Chen2, Huanfeng Jiang2.
Abstract
A highly efficient and practical synergistically metal/proton-catalyzed Conia-ene reaction for the synthesis of bicyclo[3.n.1]alkanones has been developed. This synergistic catalysis was successfully utilized in modifying natural compounds such as methyl dihydrojasmonate, α,β-thujone, and 5α-cholestan-3-one. Furthermore, the bridged carbonyl group of bicyclo[3.2.1]alkanones could be easily attacked by nucleophiles to give the ring-opened cycloheptenone products or bicyclo[4.2.1]amide in excellent yields. These reactions provide rapid access to a diverse range of cyclic structures from simple starting materials or naturally occurring compounds.Entities:
Keywords: Conia-ene reaction; bicyclo[3.n.1]alkanones; cycloheptanone; enolization; synergistic catalysis
Year: 2015 PMID: 26138939 DOI: 10.1002/anie.201504964
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336