β-Phenyl quenching of 9-phenylphenalenones: a novel photocyclisation reaction with biological implications-Reference-Cited by-同舟云学术

β-Phenyl quenching of 9-phenylphenalenones: a novel photocyclisation reaction with biological implications

Published:2014 Issue:35 Volume:16 Page:18813-18820
ISSN:1463-9076
Container-title:Phys. Chem. Chem. Phys.
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Bucher Götz¹²³⁴,Bresolí-Obach Roger⁵⁶⁷^ORCID,Brosa Carme⁵⁶⁷,Flors Cristina⁵⁶⁷⁸⁹,Luis Javier G.¹⁰¹¹¹²¹³¹¹,Grillo Teresa A.¹⁰¹¹¹²¹³¹¹,Nonell Santi⁵⁶⁷^ORCID

Affiliation:

1. WestCHEM

2. School of Chemistry

3. University of Glasgow

4. Glasgow G12 8QQ, UK

5. Institut Químic de Sarrià

6. Universitat Ramon Llull

7. Barcelona, Spain

8. IMDEA Nanociencia

9. E-28049 Madrid, Spain

10. Instituto Universitario de Bio-Orgánica “Antonio González”

11. La Laguna, Tenerife, Spain

12. Departamento de Química Orgánica

13. Facultad de Farmacia

Abstract

β-Phenyl quenching of 9-phenylphenalenones leads to the reversible formation of naphthoxanthenes and eventually to stable naphthoxanthenyl radicals or naphthoxanthenium cations.

Funder

Ministerio de Economía y Competitividad

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CP/C4CP02783C

Reference40 articles.

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

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

3. Phenalenone-Type Compounds from Musa acuminata var. “Yangambi km 5” (AAA) and Their Activity against Mycosphaerella fijiensis