Safrole and eugenol: Study of the chemical reactivity and use in the synthesis of biologically active natural products and its derivatives.

被引:42
作者
Costa, PRR [1 ]
机构
[1] Univ Fed Rio de Janeiro, Ctr Ciencias Saude, BR-12941590 Rio De Janeiro, Brazil
来源
QUIMICA NOVA | 2000年 / 23卷 / 03期
关键词
safrole; eugenol; allylbenzenes;
D O I
10.1590/S0100-40422000000300013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The chemical reactivity of safrole, eugenol, piperonal, vanillin and derivates toward ozone, aluminium chloride, brominating agents and butyl lithium was investigated, The synthesis of naturally occuring anthraquinones, furonaphthoquinones, naphthoquinones, lignans and pterocarpans from these easily available staring materials is also discussed.
引用
收藏
页码:357 / 369
页数:13
相关论文
共 105 条
[1]   Orthobromodiphenylmethane derivatives as starting materials for the total synthesis of anthraquinones [J].
Almeida, WP ;
Costa, PRR .
SYNTHETIC COMMUNICATIONS, 1996, 26 (23) :4507-4518
[2]  
ALMEIDA WP, 1990, THESIS UFRJ
[3]  
AMORIM MB, UNPUB
[4]  
AMORIM MB, 1989, THESIS UFRJ
[5]  
AMORIM MB, 1997, THESIS UFRJ
[6]  
AMORIM MB, 1987, Patent No. 59
[7]  
[Anonymous], 1972, ISOQUINOLINE ALKALOI
[8]  
[Anonymous], PHARM BASIS THERAPEU
[9]  
[Anonymous], 2017, DRUG DISCOVERY TODAY
[10]  
[Anonymous], 1969, ORGANIC CHEM SECONDA