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|Title:||The regiospecific preparation of 1,4-dioxygenated anthraquinones: a new route to islandicin, digitopurpone, and madeirin|
|Citation:||Journal of the Chemical Society, Chemical Communications, 1981; 1981(3):108-110|
|Publisher:||Royal Society of Chemistry|
|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|
|Appears in Collections:||Chemistry publications|
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