Stannyl Radical Addition-Cyclization of Oxime Ethers Connected with Olefins
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- Miyabe Hideto
- Kobe Pharmaceutical University
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- Tanaka Hirotaka
- Kobe Pharmaceutical University
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- Naito Takeaki
- Kobe Pharmaceutical University
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Abstract
Stannyl radical addition-cyclization of oxime ethers connected with olefin moieties was studied. The radical reactions proceeded effectively by the use of triethylborane as a radical initiator to provide the functionalized pyrrolidines via a carbon–carbon bond-forming process.
Journal
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- Chemical and Pharmaceutical Bulletin
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Chemical and Pharmaceutical Bulletin 52 (1), 74-78, 2004
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390001204171265792
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- NII Article ID
- 110003615480
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- NII Book ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- NDL BIB ID
- 6794859
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- PubMed
- 14709871
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed