Adelaide Research & Scholarship
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https://hdl.handle.net/2440/85866
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| Type: | Journal article |
| Title: | The regiospecific preparation of 1,4-dioxygenated anthraquinones: a new route to islandicin, digitopurpone, and madeirin |
| Author: | Russell, R.A. Warrener, R.N. |
| Citation: | Journal of the Chemical Society, Chemical Communications, 1981; 1981(3):108-110 |
| Publisher: | Royal Society of Chemistry |
| Issue Date: | 1981 |
| ISSN: | 0022-4936 |
| Statement of Responsibility: | Richard A. Russell and Ronald N. Warrener |
| Abstract: | A direct, versatile, one-step synthesis of anthraquinones which exhibits total regioselectivity (>99%) and involves the reaction of the anion of 4- or 7-methoxy-3-phenylsulphonylphthalides with variously substituted quinone monoacetals is reported. |
| Rights: | Copyright status unknown |
| DOI: | 10.1039/c39810000108 |
| Published version: | http://dx.doi.org/10.1039/c39810000108 |
| Appears in Collections: | Aurora harvest 7 Chemistry publications |
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