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- Tsugio Kitamura
- ADepartment of Chemistry and Applied Chemistry, Faculty of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan. Email: kitamura@cc.saga-u.ac.jp
書誌事項
- 公開日
- 2010-07-15
- 権利情報
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- https://doi.org/10.1071/journalslicense
- DOI
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- 10.1071/ch10072
- 10.1002/chin.201047249
- 公開者
- CSIRO Publishing
この論文をさがす
説明
<jats:p>Many methods have been developed for generating benzyne. Convenient and reliable precursors extensively studied so far involve benzenediazonium-2-carboxylate and o-dihalobenzenes such as 1,2-bromofluorobenzene and 1,2-dibromobenzene. Recently, in addition to the above precursors, o-(trimethylsilyl)phenyl triflate has been put into frequent use for benzyne reactions, in which benzyne is efficiently generated under mild conditions using fluoride ion. Furthermore, o-(trimethylsilyl)phenyliodonium triflate has been developed as a more efficient benzyne precursor. This mini-review focusses on recent progress in benzyne chemistry from the viewpoint of organic synthesis. The methods for generating benzynes are classified by the conditions into four categories: basic conditions using strong bases, mild conditions using fluoride ion, thermolysis, and oxidation.</jats:p>
収録刊行物
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- Australian Journal of Chemistry
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Australian Journal of Chemistry 63 (7), 987-1001, 2010-07-15
CSIRO Publishing
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詳細情報 詳細情報について
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- CRID
- 1361137045136443008
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- ISSN
- 14450038
- 15222667
- 00049425
- 09317597
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- データソース種別
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- Crossref
- OpenAIRE