A Convenient and Improved Procedure for the Cyanation of Enamines and 1,3-Dicarbonyl Compounds
The direct cyanation of enamines 2a-f using acylsubstituted cyanatobenzenes 1a-c and cyanatoanthraquinone 1d furnishes β-cyanoenamines 3a-f which upon hydrolysis afford the cyanoketones 4a,b. 2-Cyano-1,3-diketones 6a-c are obtained starting from compounds 5a-c and 1.
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| Veröffentlicht in: | Synthetic communications 1994-12, Vol.24 (22), p.3241-3248 |
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| container_issue | 22 |
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| container_title | Synthetic communications |
| container_volume | 24 |
| creator | Buttke, K. Niclas, H.-J. |
| description | The direct cyanation of enamines 2a-f using acylsubstituted cyanatobenzenes 1a-c and cyanatoanthraquinone 1d furnishes β-cyanoenamines 3a-f which upon hydrolysis afford the cyanoketones 4a,b. 2-Cyano-1,3-diketones 6a-c are obtained starting from compounds 5a-c and 1. |
| doi_str_mv | 10.1080/00397919408010246 |
| format | Article |
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| ispartof | Synthetic communications, 1994-12, Vol.24 (22), p.3241-3248 |
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| language | eng |
| recordid | cdi_crossref_primary_10_1080_00397919408010246 |
| source | Taylor & Francis:Master (3349 titles) |
| title | A Convenient and Improved Procedure for the Cyanation of Enamines and 1,3-Dicarbonyl Compounds |
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