期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 140, 期 48, 页码 16821-16833出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b10388
关键词
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资金
- Spanish MINECO [SAF2016-76689-R, CTQ2017-84767-P]
- Xunta de Galicia [ED431C 2017/19, 2015-CP082]
- Xunta de Galicia (Centro Singular de Investigacion de Galicia) [ED431G/09]
- ERDF, ERC [340055]
- Orfeo-Cinqa network [CTQ2016-81797-REDC]
Piperidine scaffolds are present in a wide range of bioactive natural products and are therefore considered as highly valuable, privileged synthetic targets. In this manuscript, we describe a gold-catalyzed annulation strategy that allows a straightforward assembly of piperidines and piperidine-containing aza-bridged products from readily available alkene-tethered oxime ethers (or esters) and N-allenamides. Importantly, we demonstrate the advantages of using oxime derivatives over imines, something pertinent to the whole area of gold catalysis, and provide relevant mechanistic experiments that shed light into the factors affecting the annulation processes. Moreover, we also describe preliminary experiments demonstrating the viability of enantioselective versions of the above reactions.
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