期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 78, 期 11, 页码 5711-5716出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo400419d
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资金
- National Science Council, Taiwan
In the presence of catalyst IPrAuSbF6 catalyst (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene), alkenyldiazo carbonyl species react with organic acetals to give E-configured alkyl 3,5-dimethoxy-5-pent-2-enoates stereoselectively. This reaction sequence comprises an initial Prins-type reaction, followed by gold carbene formation.
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