Synthesis of novel glycerol-derived 1,2,3-triazoles and evaluation of their fungicide, phytotoxic and cytotoxic activities

The synthesis of a series of 1,2,3-triazoles using glycerol as starting material is described. The key step in the preparation of these triazolic derivatives is the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), also known as click reaction, between 4-(azidomethyl)-2,2-dimethyl-1,3-dioxolan...

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Detalhes bibliográficos
Autores: Costa, Adilson Vidal, Oliveira, Marcos Vinicius Lacerda de, Pinto, Roberta Tristão, Moreira, Luiza Carvalheira, Gomes, Ediellen Mayara Corrêa, Alves, Thammyres de Assis, Pinheiro, Patrícia Fontes, Queiroz, Vagner Tebaldi de, Vieira, Larissa Fonseca Andrade, Teixeira, Robson Ricardo, Jesus Júnior, Waldir Cintra de
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2017
País:Brasil
Recursos:Universidade Federal de Viçosa (UFV)
Repositório:LOCUS Repositório Institucional da UFV
Idioma:inglês
OAI Identifier:oai:locus.ufv.br:123456789/16553
Acesso em linha:http://dx.doi.org/10.3390/molecules22101666
http://www.locus.ufv.br/handle/123456789/16553
Access Level:Acceso aberto
Palavra-chave:Glycerol
1,2,3-triazoles
Fungicide
Cytotoxic activity
Click chemistry
Descrição
Resumo:The synthesis of a series of 1,2,3-triazoles using glycerol as starting material is described. The key step in the preparation of these triazolic derivatives is the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), also known as click reaction, between 4-(azidomethyl)-2,2-dimethyl-1,3-dioxolane (3) and different terminal alkynes. The eight prepared derivatives were evaluated with regard to their fungicide, phytotoxic and cytotoxic activities. The fungicidal activity was assessed in vitro against Colletotrichum gloeosporioides, the causative agent of papaya anthracnose. It was found that the compounds 1-(1-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)-1H-1,2,3-triazol-4-yl)-cyclo-hexanol (4g) and 2-(1-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)-1H-1,2,3-triazol-4-yl)propan-2-ol (4h) demonstrated high efficiency in controlling C. gloeosporioides when compared to the commercial fungicide tebuconazole. The triazoles did not present any phytotoxic effect when evaluated against Lactuca sativa. However, five derivatives were mitodepressive, inducing cell death detected by the presence of condensed nuclei and acted as aneugenic agents in the cell cycle of L. sativa. It is believed that glycerol derivatives bearing 1,2,3-triazole functionalities may represent a promising scaffold to be explored for the development of new agents to control C. gloeosporioides.