Goel, Atul ; Verma, Deepti ; Singh, Fateh Veer (2005) A vicarious synthesis of unsymmetrical meta- and para- terphenyls from 2H-pyran-2-ones Tetrahedron Letters, 46 (49). pp. 8487-8491. ISSN 0040-4039
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Official URL: http://doi.org/10.1016/j.tetlet.2005.10.018
Related URL: http://dx.doi.org/10.1016/j.tetlet.2005.10.018
Abstract
An innovative synthesis of terphenyls functionalized with electron-withdrawing or -donating substituents is described and illustrated by carbanion-induced ring transformation of 2H-pyran-2-ones with 2-methoxyacetophenone in excellent yields. The existing protocols for the synthesis of terphenyls are generally inter- and intramolecular aryl–aryl cross couplings in the presence of metal complexes. In this letter, we report a potentially useful alternative to conventional metal-catalyzed cross-coupling reactions.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Terphenyl; C–C Bond; Formation; Lactone; Pyran-2-one. |
ID Code: | 117912 |
Deposited On: | 06 May 2021 08:21 |
Last Modified: | 06 May 2021 08:21 |
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