1.2.3-triazolic heterocycles: History, preparations, applications and pharmacological activities.

被引:58
作者
Melo, Julio O. F.
Donnici, Claudio Luis
Augusti, Rodinei
Ferreira, Vitor F.
de Souza, Maria Cecilia B. V.
Ferreira, Maria Lourdes G.
Cunha, Anna C.
机构
[1] Univ Estadual Minas Gerais, Ctr Univ Patos Minas, BR-38702086 Patos Minas, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Exatas, Dept Quim, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Fluminense, Inst Quim, Dept Quim Organ, BR-24020150 Niteroi, RJ, Brazil
来源
QUIMICA NOVA | 2006年 / 29卷 / 03期
关键词
1,2.3-triazoles; synthesis; applications;
D O I
10.1590/S0100-40422006000300028
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The 1.2.3-triazole, known since the end of 19(th) century, is a very widely used heterocyclic system present in many synthetic substances and commercial pharmaceutical compounds. In fact. 1,2,3-triazoles show several applications in many areas especially as medicines against many diseases like cancer, AIDS. Parkinson and Alzheimer. Nowadays there is a large variety of known methods to obtain these heterocyclic compounds comprising mainly three synthetic routes. Nevertheless, there is no article that lives an objective overview of the synthetic methods for obtaining these kinds of azoheterocycles. This paper presents a brief history of this class of compounds, and a synthetic discussion concerning the main synthetic methods for its preparation, such as cyclization through hydrazones. concerted cycloadditon [2+3] and pseudopericyclic cyclization - and some others of restricted application. but also important. Finally. this paper also provides a brief overview on pharmacological applications of some 1.2.3-triazoles.
引用
收藏
页码:569 / 579
页数:11
相关论文
共 131 条
[41]  
DIMROTH O, 1904, LIEBIGS ANN CHEM, V335, P6
[42]  
DIMROTH O, 1905, LIEBIGS ANN CHEM, V338, P154
[43]  
DZHURAEV AD, 1991, RUSS PHARM TOXICOL, V2, P140
[44]  
EBY P, 1995, HETEROCYCLES, V42, P663
[45]  
El Khadem H., 1964, J CHEM SOC, P2306
[46]   The mechanism of saccharide osotriazole formation [J].
El Khadem, HS .
CARBOHYDRATE RESEARCH, 1998, 313 (3-4) :255-257
[47]   THE SCOPE AND MECHANISM OF CARBOHYDRATE OSOTRIAZOLE FORMATION .2. THE ACTION OF OXIDISING AGENTS ON OSAZONES AND OSOTRI-AZOLES [J].
ELKHADEM, H ;
ELSHAFEI, ZM .
JOURNAL OF THE CHEMICAL SOCIETY, 1958, (SEP) :3117-3119
[48]  
ELKHADEN HS, 1960, J CHEM SOC, P3992
[49]  
ELSEKILY MA, 1993, ARAB J SCI ENG, V18, P405
[50]   Pericyclic versus pseudopericyclic 1,5-electrocyclization of iminodiazomethanes. An ab initio and density functional theory study [J].
Fabian, WMF ;
Bakulev, VA ;
Kappe, CO .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (17) :5801-5805