引用本文:
Jin Hao Zhao, Ming Hua Ji, Xu Hui Xu, Jing Li Cheng, Guo Nian Zhu. Synthesis analogues of milbemycin and their bioactivity evaluation[J]. Chinese Chemical Letters,
2010, 21(12): 1391-1394.
doi:
10.1016/j.cclet.2010.06.035
Citation: Jin Hao Zhao, Ming Hua Ji, Xu Hui Xu, Jing Li Cheng, Guo Nian Zhu. Synthesis analogues of milbemycin and their bioactivity evaluation[J]. Chinese Chemical Letters, 2010, 21(12): 1391-1394. doi: 10.1016/j.cclet.2010.06.035
Citation: Jin Hao Zhao, Ming Hua Ji, Xu Hui Xu, Jing Li Cheng, Guo Nian Zhu. Synthesis analogues of milbemycin and their bioactivity evaluation[J]. Chinese Chemical Letters, 2010, 21(12): 1391-1394. doi: 10.1016/j.cclet.2010.06.035
Synthesis analogues of milbemycin and their bioactivity evaluation
摘要:
Eight new 13-O-aminocarbonylivermectin aglycones and 4'-O-aminocarbonylivermectin monosaccharide were synthesized from ivermectin aglycone and ivermectin monosaccharide by the selective protection of C5-OH group. Their bioactivities were evaluated against spicier mites (Tetranychus cinnabarinus), aphid (Aphis fabae) and orlental armyworm (Mythimma sepatara). Their structures were confirmed by 1H NMR. MS.
English
Synthesis analogues of milbemycin and their bioactivity evaluation
Abstract:
Eight new 13-O-aminocarbonylivermectin aglycones and 4'-O-aminocarbonylivermectin monosaccharide were synthesized from ivermectin aglycone and ivermectin monosaccharide by the selective protection of C5-OH group. Their bioactivities were evaluated against spicier mites (Tetranychus cinnabarinus), aphid (Aphis fabae) and orlental armyworm (Mythimma sepatara). Their structures were confirmed by 1H NMR. MS.
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