抄録
The title carbocation, generated from 1,1-ethylene-1,6-dihydroazulene and trityl tetrafluoroborate in deuterated acetonitrile at - 20°C, was characterized by means of low temperature NMR spectroscopy, and was found to undergo expansion of the cyclopropane ring at elevated temperature and to react with nucleophiles to give the addition products at the cyclopropane methylene carbon.
本文言語 | 英語 |
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ページ(範囲) | 1011-1012 |
ページ数 | 2 |
ジャーナル | Chemistry Letters |
号 | 10 |
DOI | |
出版ステータス | 出版済み - 1997 |
ASJC Scopus 主題領域
- 化学一般