60112-44-9Relevant academic research and scientific papers
A Piperine-Based Scaffold as a Novel Starting Point to Develop Inhibitors against the Potent Molecular Target OfChtI
Deng, Ming-Fei,Duan, Hong-Xia,Han, Qing,Li, Hui-Lin,Li, Xiang,Wang, Jin-E,Wu, Nan,Yang, Qing,Zhang, Jing-Yu,Zhu, Kai
, (2021/07/26)
The insect chitinase OfChtI from the agricultural pest Ostrinia furnacalis (Asian corn borer) is a promising target for green insecticide design. OfChtI is a critical chitinolytic enzyme for the cuticular chitin degradation at the stage of molting. In thi
THE CONVERSION OF FURANS TO 2(3H)-BUTENOLIDES
Pelter, Andrew,Rowlands, Martin
, p. 1203 - 1206 (2007/10/02)
2-Aryl- and 2-alkylfurans are converted into the corresponding 5-organyl-2(3H)-butenolides by the oxidation of boron derivatives with m-chloroperbenzoic acid.
Some Observations Concerning the Lactonization of 3-Aroylpropionic Acids
Tsolomitis, A.,Sandris, C.
, p. 1545 - 1548 (2007/10/02)
The ease of lactonization og the γ-keto acids ArCOCH2CH2COOH is shown to depend on the nature of the aryl group: the presence of electron-releasing substituents on the aryl group results in a more rapid reaction as compared to the presence of electron-wit
Reactions of some Δβ,γ-Butenolides Having no Exocyclic Double bonds
Hashem, A. I.,Shaban, M. E.,El-Kafrawy, A. F.
, p. 763 - 764 (2007/10/02)
Ring-opening of γ-aryl-Δβ,γ-butenolides (I) takes place in a different manner compared to those having an exocyclic double bond at the α-position.I react with hydrazine hydrate in cold or boiling ethanol to give 6-aryl-4,5-dihydropyridazine-3(2
