1995年8月
HIGHLY SYN PI-FACIAL PREFERENCE IN THE DIELS-ALDER REACTIONS OF 1,2,3,4,5-PENTAMETHYLCYCLOPENTADIENES HAVING CARBOXY, ETHOXYCARBONYL, AND CYANO SUBSTITUENTS AT 5-POSITIONS
CHEMISTRY LETTERS
- ,
- ,
- ,
- 巻
- 1995
- 号
- 8
- 開始ページ
- 739
- 終了ページ
- 740
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1246/cl.1995.739
- 出版者・発行元
- CHEMICAL SOC JAPAN
Diels-Alder reactions of 1,2,3,4,5-pentamethylcyclopentadienes having carboxy, alkoxycarbonyl, and cyano substituents at 5-positions with N-phenymaleimide preferentially afforded the corresponding syn-attack products with the ratio of syn/anti = 80 : 20 to 100 : 0, while the diene having 5-hydroxymethyl moiety gave the anti-attack product exclusively.
- リンク情報
- ID情報
-
- DOI : 10.1246/cl.1995.739
- ISSN : 0366-7022
- Web of Science ID : WOS:A1995RR81600064