| Autor: |
Swain M; Department of Chemistry and Biochemistry, University of California─Los Angeles, Los Angeles, California 90095-1569, United States., Bunnell TB; Department of Chemistry and Biochemistry, University of California─Los Angeles, Los Angeles, California 90095-1569, United States., Kim J; Department of Chemistry and Biochemistry, University of California─Los Angeles, Los Angeles, California 90095-1569, United States., Kwon O; Department of Chemistry and Biochemistry, University of California─Los Angeles, Los Angeles, California 90095-1569, United States. |
| Abstrakt: |
In this paper, we report the synthesis of alkyl-tethered alkynes through ozone-mediated and Fe II -catalyzed dealkenylative alkynylation of unactivated alkenes in the presence of alkynyl sulfones. This one-pot reaction, which employs a combination of a catalytic Fe II salt and l-ascorbic acid, proceeds under mild conditions with good efficiency, high stereoselectivity, and broad functional group compatibility. In contrast to our previous Fe II -mediated reductive fragmentation of α-methoxyhydroperoxides, the Fe II -catalyzed process was devised through a thorough kinetic analysis of the multiple competing radical (redox) pathways. We highlight the potential of this dealkenylative alkynylation through multiple post-synthetic transformations and late-stage diversifications of complex molecules, including natural products and pharmaceuticals. |
