The regiospecific preparation of 1,4-dioxygenated anthraquinones: a new route to islandicin, digitopurpone, and madeirin
Date
1981
Authors
Russell, R.A.
Warrener, R.N.
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Journal article
Citation
Journal of the Chemical Society, Chemical Communications, 1981; 1981(3):108-110
Statement of Responsibility
Richard A. Russell and Ronald N. Warrener
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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.
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