| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218289 | Tetrahedron | 2013 | 8 Pages |
Abstract
A series of 1,3-distyrylbenzene compounds bearing different substituents at the 2-position have been synthesized and subjected to an oxidative photocyclization process. The 1,3-distyrylbenzene compounds substituted with chloro, alkylthio, and diphenylphosphino groups at the 2-position afforded dibenz[a,j]anthracene derivatives, whereas those bearing methyl, trimethylsilyl, dimethylamino, butoxy, and fluoro groups gave benzo[c]chrysene derivatives. The solubility of dibenz[a,j]anthracene in organic solvents was improved by the introduction of alkylthio groups.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Takuya Toyoshima, Satoshi Yoshida, Soichiro Watanabe,
![First Page Preview: Synthesis of an alkylthio-substituted dibenz[a,j]anthracene with improved solubility via the oxidative photocyclization of 1,3-distyrylbenzene derivatives Synthesis of an alkylthio-substituted dibenz[a,j]anthracene with improved solubility via the oxidative photocyclization of 1,3-distyrylbenzene derivatives](/preview/png/5218289.png)