Regioselective O-demethylation of two C19-diterpenoid alkaloids

被引:2
|
作者
Liang, Xiao-Xia [1 ,2 ]
Chen, Qiao-Hong [1 ]
Wang, Feng-Peng [1 ]
机构
[1] Sichuan Univ, Dept Chem Med Nat Prod, W China Coll Pharm, Chengdu 610041, Peoples R China
[2] Sichuan Agr Univ, Dept Pharm, Coll Vet, Yaan 625014, Peoples R China
基金
中国国家自然科学基金;
关键词
C-19-diterpenoid alkaloids; O-demethylation; lycoconitine; talatisamine; NORDITERPENOID ALKALOIDS; ACONITINE;
D O I
10.1080/10286020.2011.582038
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The regioselective demethylations of two C-19-diterpenoid alkaloids, 2 and 3, have been achieved with HBr-HOAc, trimethylsilyl iodide, or BBr3. It was observed that HBr-HOAc is an optimal demethylating agent for these two C-19-diterpenoid alkaloids because it could provide different O-demethylation products by using different reaction temperature and reaction time. Especially, 1-O-methyl group in 2 and 3, one of the most difficult ones to be demethylated, could be removed by the treatment with HBr-HOAc at an elevated temperature and a prolonged reaction time.
引用
收藏
页码:624 / 633
页数:10
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