Compounds > 4,8,12-trimethyl-1,3,7,11-tridecatetraene
Page last updated: 2024-09-05

4,8,12-trimethyl-1,3,7,11-tridecatetraene and Jasmone

4,8,12-trimethyl-1,3,7,11-tridecatetraene has been researched along with Jasmone in 1 studies

Compound Research Comparison

Studies
(4,8,12-trimethyl-1,3,7,11-tridecatetraene)		Trials
(4,8,12-trimethyl-1,3,7,11-tridecatetraene)		Recent Studies (post-2010)
(4,8,12-trimethyl-1,3,7,11-tridecatetraene)		Studies
(Jasmone)		Trials
(Jasmone)		Recent Studies (post-2010) (Jasmone)
70560033

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Birkett, MA; Bleicher, E; Bruce, TJ; Caulfield, JC; da Costa, JG; Dewhirst, SY; Hegde, M; Loza-Reyes, E; Mayon, P; Oliveira, JN; Pickett, JA; Santana, AE1

Other Studies

1 other study(ies) available for 4,8,12-trimethyl-1,3,7,11-tridecatetraene and Jasmone

ArticleYear
Aphid antixenosis in cotton is activated by the natural plant defence elicitor cis-jasmone.
    Phytochemistry, 2012, Volume: 78

    Topics: Acetates; Alkenes; Animals; Aphids; Cyclopentanes; Gossypium; Herbivory; Molecular Structure; Oxylipins; Salicylates; Stereoisomerism; Terpenes; Volatile Organic Compounds

2012