Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/4341
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Type: Journal article
Title: Syntheses of Angucyclinones Related to Ochromycinone. Part 3. 11-Hydroxy Isomers and Some Reduced Analogues
Author: Rozek, T.
Taylor, D.
Tiekink, E.
Bowie, J.
Citation: Australian Journal of Chemistry, 1999; 52(2):129-135
Publisher: C S I R O PUBLISHING
Issue Date: 1999
ISSN: 0004-9425
Abstract: <jats:p> The boron triacetate assisted Diels Alder reaction between racemic 5,5-dimethyl-3-vinylcyclohex- 2-enyl acetate and 5-hydroxynaphthoquinone yields the racemic 11-hydroxy-3,3-dimethyl-7,12-dioxo- 1,2,3,4,6,6a,7,12,12a,12b-decahydrobenzo[a]anthracen-1-yl acetate as the sole stereoisomer by regio- and stereo-selective cis endo addition. Aromatization of the Diels Alder adduct followed by hydrolysis of the acetate and oxidation of the resultant 1-hydroxy group gives the target angucyclinone, 11-hydroxy-3,3-dimethyl-1,2,3,4,7,12-hexahydrobenzo[a]anthracene-1,7,12-trione, in an overall yield of 37% from 5-hydroxynaphthoquinone. The regio- and stereo-selectivity of the Diels Alder addition is confirmed by a combination of 13C n.m.r. spectroscopy and X-ray crystallography.</jats:p>
RMID: 0030002816
DOI: 10.1071/C98124
Appears in Collections:Chemistry publications

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