Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Studies on Tetralin Derivatives. XI. Synthesis of 5-Hydroxy-6-acyl-1, 4-naphthoquinones
Tsutomu Momose, Shujiro Goya
Author information
JOURNAL FREE ACCESS

1959 Volume 7 Issue 8 Pages 864-866

Details
Download PDF (413K)
Download citation RIS

(compatible with EndNote, Reference Manager, ProCite, RefWorks)

BIB TEX

(compatible with BibDesk, LaTeX)

Text
How to download citation
Contact us
Abstract
The Fries rearrangement of 5, 8-dimethoxy-1-naphthol acylate gave 2-acyl-5, 8-dimethoxy-1-naphthol in a yield of 24∼56%. These acyl compounds were demethylated and oxidized to 5-hydroxy-6-acyl-1, 4-napthoquinones.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
Favorites & Alerts

Recently viewed articles
Share this page
feedback
 Top