Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/85911
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Type: Journal article
Title: Preparation of (–)-(7R)-7-acetyl-7-hydroxy-4,4-dimethoxy-5,6,7,8-tetrahydro-naphthalen-1(4H)-one, a chiral AB-synthon for anthracycline synthesis
Author: Warrener, R.
Gee, P.
Russell, R.
Citation: Journal of the Chemical Society - Series Chemical Communications, 1981; 1981(21):1100-1101
Publisher: Royal Society of Chemistry
Issue Date: 1981
ISSN: 0022-4936
Statement of
Responsibility: 
Ronald N. Warrener, Paul S. Gee and Richard A. Russell
Abstract: The (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronaphthalen-1(4H)-one (2), and the chirality at C(7) in (13) corresponds to that found at C(9) in the naturally occurring anthracyclines related to daunomycin.
Rights: Copyright status unknown
RMID: 0030009237
DOI: 10.1039/c39810001100
Appears in Collections:Chemistry publications

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