Sudarshan, Kasireddy ; Manna, Manash Kumar ; Aidhen, Indrapal Singh (2015) Synthesis of 3-Arylisocoumarins by Using Acyl Anion Chemistry and Synthesis of Thunberginol A and Cajanolactone A European Journal of Organic Chemistry, 2015 (8). pp. 1797-1803. ISSN 1434-193X
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Official URL: http://doi.org/10.1002/ejoc.201403524
Related URL: http://dx.doi.org/10.1002/ejoc.201403524
Abstract
3-Arylisocoumarins are synthesized by using a new strategy based on acyl anion chemistry. Aryl-substituted α-aminonitriles are used as acyl anion equivalents in this study. Further, the route is general and can be applied to the synthesis of 8-hydroxy-3-arylisocoumarins, including thunberginol A and cajanolactone A, which are naturally occurring isocoumarins known for their biological activities. DBU = 1,8-diazabicyclo[5.4.0]undec-7-ene.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to John Wiley and Sons. |
| ID Code: | 131874 |
| Deposited On: | 09 Dec 2022 06:36 |
| Last Modified: | 09 Dec 2022 06:36 |
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