Larvicidal and structure–activity studies of natural phenylpropanoids and their semisynthetic derivatives against the tobacco armyworm Spodoptera litura (Fab.)( …
A Bhardwaj, D Kumar Tewary, R Kumar…
Index: Bhardwaj, Anu; Tewary, Dhananjay Kumar; Kumar, Rakesh; Kumar, Vinod; Sinha, Arun Kumar; Shanker, Adarsh Chemistry and Biodiversity, 2010 , vol. 7, # 1 p. 168 - 177
Full Text: HTML
Citation Number: 18
Abstract
Abstract The larvicidal activity of 18 phenylpropanoids, 1–18, including phenylpropenoate, phenylpropenal, phenylpropene, and their semisynthetic analogues, were evaluated against the tobacco armyworm, Spodoptera litura (Fab.), to identify promising structures with insecticidal activity. Amongst various phenylpropanoids, isosafrole, a phenylpropene, showed the best activity, with an LC 50 value of 0.6 μg/leaf cm 2, followed by its ...
Related Articles:
Exploring the scope for scale-up of organic chemistry using a large batch microwave reactor
[Schmink, Jason R.; Kormos, Chad M.; Devine, William G.; Leadbeater, Nicholas E. Organic Process Research and Development, 2010 , vol. 14, # 1 p. 205 - 214]
An Improved Bouveault− Blanc Ester Reduction with Stabilized Alkali Metals
[Bodnar, Brian S.; Vogt, Paul F. Journal of Organic Chemistry, 2009 , vol. 74, # 6 p. 2598 - 2600]
[Zhu, Maiyong; Wang, Ying; Wang, Chengjiao; Li, Wei; Diao, Guowang Catalysis Science and Technology, 2013 , vol. 3, # 4 p. 952 - 961]
[Nabid, Mohammad Reza; Bide, Yasamin Applied Catalysis A: General, 2014 , vol. 469, p. 183 - 190]
Aryliodine (III) diacetates as substrates for Pd–Ag catalyzed arylation of alkenes
[Evdokimov, Nikolai M.; Kornienko, Alexander; Magedov, Igor V. Tetrahedron Letters, 2011 , vol. 52, # 33 p. 4327 - 4329]