1 |
徐小俊, 黄媛媛, 晁骏, 等. 热带优势作物农药使用减量增效对策建议[J]. 中国植保导刊, 2019, 39 (8): 77- 81.
doi: 10.3969/j.issn.1672-6820.2019.08.019
|
2 |
李友顺, 白小宁, 袁善奎, 等. 2019年及近年我国农药登记情况和特点分析[J]. 农药科学与管理, 2021, 41 (3): 14- 24.
|
3 |
王以燕, 袁善奎, 农向群, 等. 我国微生物农药常见剂型种类及管理[J]. 中国生物防治学报, 2021, 37 (4): 640- 645.
doi: 10.16409/j.cnki.2095-039x.2021.07.011
|
4 |
BALCERZAK L , LOCHYÑSKI S , LIPOK J . Influence of monoterpenoids on the growth of freshwater cyanobacteria[J]. Applied Microbiology and Biotechnology, 2021, 105 (13): 5675- 5687.
doi: 10.1007/s00253-021-11260-8
|
5 |
PINHEIRO P F , COSTA A V , ALVES T , et al. Phytotoxicity and cytotoxicity of essential oil from leaves of plectranthus amboinicus, carvacrol, and thymol in plant bioassays[J]. Journal of Agricultural & Food Chemistry, 2015, 63 (41): 8981- 8990.
|
6 |
GOUDA N , SAAD M , ABDELGALEIL S . PRE and post herbicidal activity of monoterpenes against barnyard grass(Echinochloa crus-galli)[J]. Weed Science, 2017, 64 (1): 191- 200.
|
7 |
UMEMOTO K , NAGASAWA T . Absolute configuration of a new monoterpenic diol isolated from essential oil of Mentha gentilis L.(Studies on chemical constituents of wild mints Part X)[J]. Journal of the Agricultural Chemical Society of Japan, 1977, 51 (4): 245- 251.
|
8 |
LEITO S G , MARTINS G R , FRUCTUOSO L M , et al. Absolute stereochemistry of antifungal limonene-1, 2-diols from Lippia rubella[J]. Revista Brasileira de Farmacognosia, 2020, 30 (4): 537- 537.
doi: 10.1007/s43450-020-00081-x
|
9 |
NISHIMURA H , KAKU K , NAKAMURA T , et al. Allelopathic substances, (±)-p-menthane-3, 8-diols isolated from eucalyptus citriodora hook[J]. Journal of the Agricultural Chemical Society of Japan, 1982, 46 (1): 319- 320.
|
10 |
田玉红, 刘雄民, 周永红, 等. 柠檬桉叶挥发性成分的提取及成分分析[J]. 色谱, 2005, 23 (6): 651- 654.
doi: 10.3321/j.issn:1000-8713.2005.06.018
|
11 |
何丽芝, 赵振东, 毕良武, 等. 对孟烷-3, 8-二醇的合成与应用研究进展[J]. 天然产物研究与开发, 2012, 24 (8): 1147- 1150.
doi: 10.3969/j.issn.1001-6880.2012.08.030
|
12 |
KURNIA I , YOSHIDA A , CHAIHAD N , et al. Synthesis of p-menthane-3, 8-diol from citronellal over lignin-derived carbon acid catalysts[J]. New Journal of Chemistry, 2020, 44 (25): 10441- 10447.
doi: 10.1039/D0NJ00919A
|
13 |
BANDRES M , CARO P D , THIEBAUDROUX S , et al. Green synthesis of para-menthane-3, 8-diol from Eucalyptus citriodora: Application for repellent products[J]. Comptes Rendus Chimie, 2011, 14 (7/8): 629- 635.
|
14 |
BARNARD D R , XUE R D . Laboratory evaluation of mosquito repellents against Aedes albopictus, Culex nigripalpus, and Ochlerotatus triseriatus(Diptera: Culicidae)[J]. Journal of Medical Entomology, 2004, 41 (4): 726- 730.
doi: 10.1603/0022-2585-41.4.726
|
15 |
王婧, 杨学兵赵振东, 等. 3-蒈烯催化转化反应及应用研究[J]. 林产化学与工业, 2017, 37 (1): 36- 42.
|
16 |
孙小玲, 江营, 陈萍, 等. 一种蚊蝇趋避剂3, 4-蒈二醇的制备方法: 中国CN102060671 A[P]. 2010-12-16.
|
17 |
SEMBO S. Carane-3, 4-diol insect growth regulators and insecticides: US20040176368 A1[P]. 2002-02-12.
|
18 |
MAKITA M, MATSUNAGA T. Pest repellent composition: US6528078 B1[P]. 2003-03-04.
|
19 |
黄道战, 甄月文, 朱守记, 等. 过氧磷钼钨酸盐高效催化3-蒈烯氧化合成3, 4-环氧蒈烷[J]. 精细化工, 2014, 31 (12): 1526- 1530.
|
20 |
武怀恒, 万鹏, 黄民松. 毒力回归计算方法及相应软件使用介绍[J]. 安徽农业科学, 2014, 42 (27): 9335- 9338.
doi: 10.3969/j.issn.0517-6611.2014.27.030
|
21 |
KOLEHMAINEN E , LAIHIA K , HEINAENEN M , et al. Oxygen-containing bicyclic monoterpenes.1H, 13C and 17O NMR Spectroscopic and X-ray diffraction studies of seven oxidation products of(+)-3-carene[J]. Journal of the Chemical Society, Perkin Transactions, 1993, 2 (4): 641- 648.
|
22 |
LORENZO G B , NIRYHASINANDRIANINA R , ERWANN J , et al. Effect of the stereoselectivity of para-menthane-3, 8-diol isomers on repulsion toward Aedes albopictus[J]. Journal of Agricultural & Food Chemistry, 2021, 69 (37): 11095- 11109.
|