2000
DOI: 10.1021/bk-2000-0754.ch016
|View full text |Cite
|
Sign up to set email alerts
|

Radical Scavenging Mechanisms of Catechins on 2,2-Diphenyl-1-picrylhydrazyl Radical

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2005
2005
2010
2010

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…Two research groups have already presented a similar reaction mechanism between tea catechin and a DPPH radical. 15,16) In the case of catechin, the ortho dihydroxy structure was converted into ortho quinone, but not into quinone methide. Accordingly, aspernolide A is the first compound we can assume to be transformed to a quinone methide by the reaction with two molecules of the DPPH radical.…”
Section: )mentioning
confidence: 99%
“…Two research groups have already presented a similar reaction mechanism between tea catechin and a DPPH radical. 15,16) In the case of catechin, the ortho dihydroxy structure was converted into ortho quinone, but not into quinone methide. Accordingly, aspernolide A is the first compound we can assume to be transformed to a quinone methide by the reaction with two molecules of the DPPH radical.…”
Section: )mentioning
confidence: 99%