Application In Synthesis of 1,1,1-Triethoxyethane. In 2019.0 CHEM BIODIVERS published article about CLAISEN REARRANGEMENT; LACTONES; KETONES in [Koziol, Agata; Jasnowski, Mateusz; Grela, Ewa; Lochynski, Stanislaw] Wroclaw Univ Sci & Technol, Dept Bioorgan Chem, Wyb Wyspianskiego 27, PL-50370 Wroclaw, Poland; [Koziol, Agata; Lochynski, Stanislaw] Wroclaw Coll Physiotherapy, Inst Cosmetol, Kosciuszki 4, PL-50038 Wroclaw, Poland; [Szczepanik, Maryla] Nicolaus Copernicus Univ, Dept Invertebrate Zool, Lwowska 1, PL-87100 Torun, Poland; [Gabrys, Beata; Dancewicz, Katarzyna] Univ Zielona Gora, Fac Biol Sci, PL-65516 Szafrana, Zielona Gora, Poland in 2019.0, Cited 31.0. The Name is 1,1,1-Triethoxyethane. Through research, I have a further understanding and discovery of 78-39-7.
In the synthesis performed in this study, derivatives of 4-tert-butylcyclohexanone 1 were obtained using typical reactions of organic synthesis. The bioactivity of the selected compounds was evaluated. 1-(Bromomethyl)-8-tert-butyl-2-oxaspiro[4.5]decan-3-one (5) was characterized by attractant properties against larvae and a weak feeding deterrent activity against adults of Alphitobius diaperinus Panzer. This bromolactone was a moderate antifeedant towards Myzus persicae Sulzer. In addition, ethyl (4-tert-butylcyclohexylidene)acetate (2) and bromolactone 5 displayed antibacterial activity. The strongest bacteriostatic effect was observed against Gram-positive strains: Bacillus subtilis and Staphylococcus aureus. The bromolactone 5 also limited the growth of Escherichia coli strain.
Welcome to talk about 78-39-7, If you have any questions, you can contact Koziol, A; Jasnowski, M; Grela, E; Szczepanik, M; Gabrys, B; Dancewicz, K; Lochynski, S or send Email.. Application In Synthesis of 1,1,1-Triethoxyethane
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