Abstract
The novel metacyclophanes with chalcone moieties were synthesized by Claisen-Schmidt condensation. These α,β-unsaturated ketones were photoisomerized from the all-trans configuration to the partial trans configuration by 365 nm light irradiation, and then, these cis photoisomers were thermally reversed
Keywords: α, β-unsaturated ketone, Aldol reaction, chalcone, Claisen-Schmidt condensation, metacyclophane, photoisomerization
Letters in Organic Chemistry
Title:Syntheses of Novel Planar Metacyclophanes by Claisen-Schmidt Condensation and Thermal Stabilities of Their Photoisomers
Volume: 9 Issue: 10
Author(s): Ken Ishikawa, Hiroshi Katagiri, Kazuo Tsujimoto and Yoshihiro Ohba
Affiliation:
Keywords: α, β-unsaturated ketone, Aldol reaction, chalcone, Claisen-Schmidt condensation, metacyclophane, photoisomerization
Abstract: The novel metacyclophanes with chalcone moieties were synthesized by Claisen-Schmidt condensation. These α,β-unsaturated ketones were photoisomerized from the all-trans configuration to the partial trans configuration by 365 nm light irradiation, and then, these cis photoisomers were thermally reversed
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Cite this article as:
Ishikawa Ken, Katagiri Hiroshi, Tsujimoto Kazuo and Ohba Yoshihiro, Syntheses of Novel Planar Metacyclophanes by Claisen-Schmidt Condensation and Thermal Stabilities of Their Photoisomers, Letters in Organic Chemistry 2012; 9 (10) . https://dx.doi.org/10.2174/157017812803901971
DOI https://dx.doi.org/10.2174/157017812803901971 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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