期刊
ORGANIC LETTERS
卷 11, 期 24, 页码 5618-5620出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol902339a
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资金
- JSPS [21350020, 21750086]
- Grants-in-Aid for Scientific Research [21350020, 21750086] Funding Source: KAKEN
The Rh-catalyzed coupling reaction between propargylic carbonates and a silylboronate afforded allenylsilanes with different substitution patterns in high yields. The reaction tolerates a variety of functional groups in propargylic carbonates. The reaction of an optically active propargylic carbonate proceeded with excellent chirality transfer with 1,3-anti stereochemistry to give an axially chiral allenylsilane.
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