34495-35-7Relevant academic research and scientific papers
Synthesis and Insecticidal Activity of N-Oxydihydropyrroles: 4-Hydroxy-3-mesityl-5,5-dimethyl Derivatives with Various Substituents at the 1-Position
Iro, Mitsuru,Okui, Hideshi,Nakagawa, Harumi,Mio, Shigeru,Kinoshita, Ayako,Obayashi, Takashi,Miura, Takako,Nagai, Junko,Yokoi, Shinji,Ichinose, Reiji,Tanaka, Keiji,et al.
, p. 2406 - 2414 (2007/10/03)
A new series of N-oxydihydropyrrole derivatives was synthesized and evaluated for insecticidal activity against Nilaparvata lugens and Myzus persicae. Various substituents were introduced to the 1-position of the dihydropyrrole ring, and the derivatives obtained exhibited systemic and/or contact insecticidal activity. The structure-activity relationship revealed that small alkyoxy and alkoxyalkoxy groups were more favorable than alkylcarbonyloxy, alkoxycarbonyloxy, or sulfonyloxy groups as substituents at the 1-position.
Synthesis of N-oxydihydropyrrole derivatives
Ito, Mitsuru,Okui, Hideshi,Nakagawa, Harumi,Mio, Shigeru,Iwasaki, Toshiaki,Iwabuchi, Jun
, p. 881 - 894 (2007/10/03)
N-Oxydihydropyrrole derivatives were synthesized through an intramolecular Claisen condensation reaction. The N-acylation of hindered hydroxylamines played a key role in providing the useful intermediates, which could be converted to a variety of N-oxydihydropyrrole derivatives.
