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紫苏醛基席夫碱-(硫)脲化合物的合成及生物活性

马媛 段文贵 林桂汕 刘陆智 黄正松 雷福厚

林产化学与工业2017,Vol.37Issue(1):54-62,9.
林产化学与工业2017,Vol.37Issue(1):54-62,9.DOI:10.3969/j.issn.0253-2417.2017.01.007

紫苏醛基席夫碱-(硫)脲化合物的合成及生物活性

Synthesis and Biological Activities of Perillaldehyde-based Schiff Base-(thio)urea Compounds

马媛 1段文贵 1林桂汕 1刘陆智 1黄正松 1雷福厚2

作者信息

  • 1. 广西大学 化学化工学院, 广西 南宁 530004
  • 2. 广西林产化学与 工程重点实验室, 广西 南宁 530008
  • 折叠

摘要

Abstract

Thirteen novel perillaldehyde-based Schiff base-(thio)urea compounds (5a-5m) were designed and synthesized by using perillaldehyde as starting material.Their structures were analyzed and characterized by FT-IR, 1H NMR, 13C NMR, and ESI-MS.The results of preliminary bioassay showed that, at the mass concentration of 50 mg/L, the inhibition rate of target compound 5f (R=p-FAr) against Physalospora piricola was 90.0% (close to that of the positive control azoxystrobin), and the inhibition rate of target compound 5d (R=Ar) against Alternaria solani was 91.8% (close to that of the positive control azoxystrobin).Besides, at the mass concentration of 100 mg/L, the target compounds 5c (R=cyclopentyl), 5i (R=p-CH3Ar) and 5a (R=CH3) exhibited 77.6%, 75.3% and 67.4% inhibition against the growth of rape (Brassica campestris) root, respectively (greater than positive control flumioxazin).Furthermore, substituted phenyl thioureas showed better antifungal and herbicidal activities than substituted phenyl ureas.

关键词

紫苏醛/席夫碱-(硫)脲/合成/抑菌活性/除草活性

Key words

perillaldehyde/Schiff base-(thio)urea/synthesis/antifungal activity/herbicidal activity

分类

化学化工

引用本文复制引用

马媛,段文贵,林桂汕,刘陆智,黄正松,雷福厚..紫苏醛基席夫碱-(硫)脲化合物的合成及生物活性[J].林产化学与工业,2017,37(1):54-62,9.

基金项目

国家自然科学基金资助项目(31460173) (31460173)

广西林产化学与工程重点实验室开放基金资助项目(GXFC15-01) (GXFC15-01)

广西大学"大学生创新创业训练计划"资助项目(201510593002) (201510593002)

林产化学与工业

OA北大核心CSCDCSTPCD

0253-2417

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