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Thermal ring opening of tricyclobutabenzenes into hexaradialenes
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- Shinozaki Shinya
- Tokyo Institute of Techonology SORST
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- Hamura Toshiyuki
- Kwansei Gakuin University PRESTO
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- Ibusuki Yousuke
- Tokyo Institute of Techonology SORST
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- Suzuki Keisuke
- Tokyo Institute of Techonology SORST
Bibliographic Information
- Other Title
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- トリシクロブタベンゼンの熱的開環によるヘキサラジアレンの合成
Description
We previously developed an efficient access to highly functionalized tricyclobutabenzenes via repeated [2+2] cycloaddition of benzyne and ketene silyl acetal. Experimental study on these strained compounds revealed that they were easily converted to the corresponding valence isomer, hexaradialene. Furthermore, it turned out that the reaction was influenced by the substituents on the four-membered ring, which is discussed in this presentation. Also discussed will be the X-ray structure of the hexaradialene.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 2008 (0), 7-7, 2008
The Society of Physical Organic Chemistry, Japan
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Details 詳細情報について
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- CRID
- 1390282680533513984
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- NII Article ID
- 130004645556
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed