Bhalla, Vandana ; Singh, Hardev ; Kumar, Manoj (2010) Facile cyclization of terphenyl to triphenylene: A new chemodosimeter for fluoride ions Organic Letters, 12 (3). pp. 628-631. ISSN 1523-7060
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Official URL: https://pubs.acs.org/doi/abs/10.1021/ol902861b
Related URL: http://dx.doi.org/10.1021/ol902861b
Abstract
Terphenyl derivatives 3 and 4 having OTBS groups have been synthesized via a Suzuki−Miyura coupling reaction. These compounds undergo unprecedented irreversible cyclization to symmetrically/unsymmetrically substituted triphenylenes while carrying out the deprotection of OTBS groups using tetrabutylammonium fluoride. Terphenyl 3 also serves as a new chemodosimeter for fluoride ions.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 114453 |
Deposited On: | 18 May 2018 08:48 |
Last Modified: | 18 May 2018 08:48 |
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