[4+2] cycloaddition of intermediates generated from arynes and DMF
書誌事項
- 公開日
- 2014-02
- 資源種別
- journal article
- 権利情報
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- https://www.elsevier.com/tdm/userlicense/1.0/
- https://www.elsevier.com/legal/tdmrep-license
- DOI
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- 10.1016/j.tetlet.2013.12.119
- 公開者
- Elsevier BV
この論文をさがす
説明
The trapping reaction of the transient intermediate ortho-quinone methides, generated by the insertion of arynes into a carbon–oxygen double bond of DMF, with dienophiles was investigated. The [4+2] cycloaddition products were obtained when the diesters of acetylenedicarboxylic acid were employed as dienophiles.
収録刊行物
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- Tetrahedron Letters
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Tetrahedron Letters 55 (8), 1402-1405, 2014-02
Elsevier BV
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詳細情報 詳細情報について
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- CRID
- 1360848657457688960
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- ISSN
- 00404039
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- 資料種別
- journal article
-
- データソース種別
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- Crossref
- KAKEN
- OpenAIRE