Regio- and stereoselective functionalizations of the Wieland-Miescher ketone derivatives at the C-8 position.
Abstract
New efficient methods for stereoselective hydroxymethylation, hydroxylation, and thiophenylation at the C-8 position of the Wieland-Miescher ketone derivatives (2__--4__-) have been developed by diverse modifications from the Kirk-Petrow reaction, which involve autoxidation for the hydroxylation.
Journal
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- Chemical and Pharmaceutical Bulletin
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Chemical and Pharmaceutical Bulletin 37 (7), 1963-1965, 1989
The Pharmaceutical Society of Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390001204167405568
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- NII Article ID
- 130003771695
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- ISSN
- 13475223
- 00092363
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed