Please use this identifier to cite or link to this item: http://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
RMID: 0030009162
DOI: 10.1039/c39810000108
Appears in Collections:Chemistry publications

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