Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/86029
Citations | ||
Scopus | Web of Science® | Altmetric |
---|---|---|
?
|
?
|
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, 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 |
DOI: | 10.1039/c39830000994 |
Published version: | http://dx.doi.org/10.1039/c39830000994 |
Appears in Collections: | Aurora harvest 7 Chemistry publications |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.