摘要
本文以取代氯(溴)苄、对羟基苯甲醛、甲胺或异丙胺为原料,经过O烷基化、还原胺化及N-烷基化反应,制备了15个未见文献报道的化合物,其结构经IR、1HNMR及元素分析予以确证。初步生物活性实验表明,所有化合物在浓度为100mg/L时对小麦赤霉病菌(Fusari umgraminearum)有不同程度的抑制作用。
Fifteen compounds were synthesized through benzylchloride, р-hydroxy benzaldehyde methylamine or isopropylamine by O-alkylation Reductive-ammination and N-alkylation. The structures were confirmed by ~1HNMR, IR and elementary analysis. The preliminary bioassays showed all compounds exhibited certain fungicidal activity.
出处
《西北林学院学报》
CSCD
北大核心
2005年第2期164-166,共3页
Journal of Northwest Forestry University
基金
西北农林科技大学青年基金(KD0056)
