Mahal, Ahmed and Villinger, Alexander and Langer, Peter (2011) Site-Selective Arylation of Alizarin and Purpurin Based on Suzuki–Miyaura Cross-Coupling Reactions. European Journal of Organic Chemistry, 2011 (11). pp. 2075-2087. ISSN 1099-0690 (online)
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Abstract
A variety of arylated anthraquinones were prepared by site-selective Suzuki–Miyaura cross-coupling reactions of the bis- and tris(triflates) of alizarin and purpurin, respectively. The site-selectivity is controlled by the electronic influence of the carbonyl group and by steric parameters.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Arylated anthraquinones, Suzuki–Miyaura cross-coupling, Site-selectivity, Alizarin and purpurin derivatives, Electronic and steric effects |
| Subjects: | Q Science > QD Chemistry Q Science > QK Botany T Technology > TP Chemical technology |
| Divisions: | Department of Medical Biochemical Analysis > Research papers |
| Depositing User: | ePrints Depositor |
| Date Deposited: | 21 Aug 2025 05:02 |
| Last Modified: | 21 Aug 2025 05:02 |
| URI: | https://eprints.cihanuniversity.edu.iq/id/eprint/4923 |
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