Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/86029
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Type: Journal article
Title: An economical and versatile synthesis of 5,8-dialkoxy-2-acetyl-3,4-dihydronaphthalenes: key precursors for the synthesis of chiral anthracyclines
Author: Russell, R.A.
Collin, G.J.
Gee, P.S.
Warrener, R.N.
Citation: Journal of the Chemical Society - Series Chemical Communications, 1983; 1983(18):994-995
Publisher: Royal Society of Chemistry
Issue Date: 1983
ISSN: 0022-4936
Statement of
Responsibility: 
Richard A. Russell, Geoffrey J. Collin, Paul S. Gee and Ronald N. Warrener
Abstract: 5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct of buta-1,3-diene and p-benzoquinone, is selectively deacetylated (Cs2CO3 in tetrahydrofuran or K2CO3 in dimethyl sulphoxide) to intermediates suitable for use in chiral anthracycline synthesis.
Rights: Copyright status unknown
RMID: 0030009209
DOI: 10.1039/c39830000994
Appears in Collections:Chemistry publications

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