Papers

2000

Regioselective preparation of 1,6- and 1,8-dihydroxy-9,10-anthraquinones from the common intermediates: Synthesis of aloesaponarin I and K1115A

Chemistry Letters
  • Hidemitsu Uno
  • ,
  • Yumi Nagamachi
  • ,
  • Erina Honda
  • ,
  • Akane Masumoto
  • ,
  • Noboru Ono

Volume
Number
9
First page
1014
Last page
1015
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1246/cl.2000.1014
Publisher
Chemical Society of Japan

Treatment of 3-acyl-2-[(2,2-dimethyl-6-oxo-1,3-dioxin-4-yl)methyl]-5-methoxy-1,4-naphthoquino nes with K2CO3 in an alcohol brought about the intramolecular condensation to give 1-alkyl-3-hydroxy-8-methoxy-9,10-anthraquinone-2-carboxy-lates in good yields, while the same naphthoquinone gave 1-hydroxy-8-methoxy-9,10-anthraquinone-3-acetic acid in good yield by treatment with KHMDS.

Link information
DOI
https://doi.org/10.1246/cl.2000.1014
CiNii Articles
http://ci.nii.ac.jp/naid/10004695513
URL
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0034339913&origin=inward
ID information
  • DOI : 10.1246/cl.2000.1014
  • ISSN : 0366-7022
  • CiNii Articles ID : 10004695513
  • SCOPUS ID : 0034339913

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