論文

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
  • M ISHIDA
  • ,
  • S TOMOHIRO
  • ,
  • M SHIMIZU
  • ,
  • S INAGAKI

1995
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
DOI
https://doi.org/10.1246/cl.1995.739
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:A1995RR81600064&DestApp=WOS_CPL
ID情報
  • DOI : 10.1246/cl.1995.739
  • ISSN : 0366-7022
  • Web of Science ID : WOS:A1995RR81600064

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