2013年7月31日
Synthesis of 2,3,4,5-tetra-substituted pyrroles via a base-promoted double Michael reaction of oxime-enoates with nitroolefins
Tetrahedron Letters
- ,
- ,
- ,
- ,
- 巻
- 54
- 号
- 31
- 開始ページ
- 4073
- 終了ページ
- 4075
- 記述言語
- 英語
- 掲載種別
- 研究論文（学術雑誌）
- DOI
- 10.1016/j.tetlet.2013.05.100
- 出版者・発行元
- Elsevier BV
A new method of synthesizing 2,3,4,5-tetra-substituted pyrroles from oxime-enoates with nitroolefins is described. This reaction involves a base-promoted double Michael reaction, followed by dehydrative aromatization. © 2013 Elsevier Ltd. All rights reserved.
- ID情報
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- DOI : 10.1016/j.tetlet.2013.05.100
- ISSN : 0040-4039
- ISSN : 1873-3581
- ORCIDのPut Code : 43398937
- SCOPUS ID : 84879688460