Diastereoselective Solid-Phase Radical Addition to Oxime Ether Anchored to Polymer Support
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- Miyabe Hideto
- Kobe Pharmaceutical University
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- Konishi Chihiro
- Kobe Pharmaceutical University
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- Naito Takeaki
- Kobe Pharmaceutical University
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Abstract
Stereocontrol in radical reactions of oxime ether anchored to polymer support was studied. Highly diastereoselective solid-phase radical reaction was achieved by using triethylborane and diethylzinc as a radical initiator at low reaction temperature, providing a novel method for the synthesis of the α-amino acid derivatives with excellent diastereoselectivities.
Journal
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- Chemical and Pharmaceutical Bulletin
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Chemical and Pharmaceutical Bulletin 51 (5), 540-544, 2003
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390282679139077504
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- NII Article ID
- 110003615345
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- NII Book ID
- AA00602100
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- COI
- 1:CAS:528:DC%2BD3sXltVejs7Y%3D
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- ISSN
- 13475223
- 00092363
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- NDL BIB ID
- 6517028
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- PubMed
- 12736453
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed