9-Iodophenalenone and 9-trifluoromethanesulfonyloxyphenalenone: convenient entry points to new phenalenones functionalised at the 9-position. Iodine-carbonyl interaction studies by X-ray crystallography-Reference-Cited by-同舟云学术

9-Iodophenalenone and 9-trifluoromethanesulfonyloxyphenalenone: convenient entry points to new phenalenones functionalised at the 9-position. Iodine-carbonyl interaction studies by X-ray crystallography

Published:2014 Issue:100 Volume:4 Page:56654-56657
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Anamimoghadam Ommid¹²³⁴,Long De-Liang¹²³⁴,Bucher Götz¹²³⁴

Affiliation:

1. WestCHEM

2. School of Chemistry

3. University of Glasgow

4. Glasgow G12 8QQ, UK

Abstract

Triflic anhydride acts like a key to the unreactive, “locked” 9-hydroxyphenalenone, providing access to new phenalenones functionalised in 9-position as well as to a phenalenyl-annelated isoxazole.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA00178H

Reference33 articles.

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4. Light- and singlet oxygen-mediated antifungal activity of phenylphenalenone phytoalexins

5. Light and Singlet Oxygen in Plant Defense Against Pathogens: Phototoxic Phenalenone Phytoalexins

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