Synthesis Of Triazoles
Mostrando 13-24 de 28 artigos, teses e dissertações.
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13. Ultrasound-Assisted Synthesis of Isatin-Type 5'-(4-Alkyl/Aryl-1H-1,2,3-triazoles) via 1,3-Dipolar Cycloaddition Reactions
This short report describes the preparation of twelve isatin derivatives, 5'-(4-alkyl/aryl-1H-1,2,3-triazoles), using 5-azido-spiro[1,3-dioxolane-2,3'-indol]-2'(1'H)-one in the presence of various alkynes under acidic conditions and ultrasound irradiation. Compared with conventional methods, yields increased to 78-98%, and reaction times decreased to 5 min.
J. Braz. Chem. Soc.. Publicado em: 2016-12
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14. Combining the Pharmacophore Features of Coumarins and 1,4-Substituted 1,2,3-Triazoles to Design New Acetylcholinesterase Inhibitors: Fast and Easy Generation of 4-Methylcoumarins/1,2,3-triazoles Conjugates via Click Chemistry
Coumarins are a large class of compounds that display a range of interesting biological properties, being considered privileged structures because of the ability of their 2H-chromen-2-one nuclei to bind to multiple pharmacological targets. We hypothesized that the linkage of a second pharmacophore nucleus to the 2H-chromen-2-one core, the 1,2,3-triazole moie
J. Braz. Chem. Soc.. Publicado em: 2016-09
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15. Synthesis, in vitro Antimalarial Activity and in silico Studies of Hybrid Kauranoid 1,2,3-Triazoles Derived from Naturally Occurring Diterpenes
We herein report the synthesis of hybrid kauranoid molecules of type 1,2,3-triazole-1,4-disubstituted aiming to improve the antimalarial activity of kaurenoic and xylopic acids. The CuI-catalyzed cycloaddition of azides and kauranoid terminal alkynes was explored as a hybridization strategy. Kauranoid terminal alkynes were prepared from kaurenoic and xylopic
J. Braz. Chem. Soc.. Publicado em: 2016-03
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16. Efficient Eco-Friendly Solvent-Free Click Synthesis and Antimicrobial Evaluation of New Fluorinated 1,2,3-Triazoles and their Conversion into Schiff Bases
A facile and convenient green click synthesis has been developed for the preparation of new fluorinated 1,2,3-triazoles under solvent-free conditions via a Huisgen 1,3-dipolar cycloaddition reaction between dimethylacetylene dicarboxylate (DMADC) and fluorophenyl azides in excellent yields within 2 min. Treatment of the resulting diesters with hydrazine hydr
J. Braz. Chem. Soc.. Publicado em: 2015-10
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17. On the search for potential antimycobacterial drugs: synthesis of naphthoquinoidal, phenazinic and 1,2,3-triazolic compounds and evaluation against mycobacterium tuberculosis
Fifteen naphthoquinones, sixteen phenazines and fifteen aryl triazoles were synthesized and evaluated against Mycobacterium tuberculosis. Twenty five substances are reported here for the first time and, among all of the compounds evaluated, six presented MIC (minimal inhibitory concentration) values < 6.25 µg mL-1. These substances are promising antimycobac
J. Braz. Chem. Soc.. Publicado em: 2015-05
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18. Synthesis of novel isatin-type 5'-(4-Alkyl/Aryl-1H-1,2,3-triazoles) via 1,3-dipolar cycloaddition reactions
As isatinas e os 1H-1,2,3-triazóis são duas classes de compostos com grande destaque na síntese orgânica e na química medicinal uma vez que são núcleos heterociclos com elevada reatividade, que permitem a obtenção de diversos compostos com importantes propriedades biológicas. Neste artigo, a síntese de novos 5`-(4-alquil/aril-1H-1,2,3-triazóis)-i
J. Braz. Chem. Soc.. Publicado em: 2013-02
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19. Síntese de 4-organocalcogenoil-1H-1,2,3-triazol: funcionalização da unidade triazólica via acoplamento de Negishi catalisado por níquel / 4-Organochalcogenoyl-1H-1,2,3-triazole synthesis: functionalization of the triazole scaffold by nickel-catalyzed Negishi cross-coupling
No presente trabalho, uma série de calcogenotriazóis (3a-o,5a-f) foi sintetizada empregando reações de cicloadição entre azidas e alquinos catalisadas por cobre (CAACu), com duas diferentes metodologias: uma aplicada aos selenetos e outra aos teluretos triazólicos. Os selenetos acetilênicos (1a,b) foram submetidos ao sistema catalítico Cu(OAc)2/asco
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 16/08/2012
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20. Synthesis of N-substituted phthalimidoalkyl 1H-1,2,3-triazoles: a molecular diversity combining click chemistry and ultrasound irradiation
Uma série de derivados 1,2,3-triazólicos foi sintetizada a partir de N-alquilftalimida-azidas (A1 -A4) e alcinos (a-e) sob irradiação de ultrassom na presença de CuI, Et3N e DMF como solvente. O presente protocolo forneceu 18 novos 1,2,3-triazóis (1-4) em rendimentos de bons a excelentes (67-98%).
J. Braz. Chem. Soc.. Publicado em: 19/10/2012
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21. Efficient synthesis of functionalized 1,2,3-triazoles by catalyst-free 1,3-dipolar cycloaddition of nitroalkenes with sodium azide
Foi desenvolvido um protocolo simples e eficiente para a síntese de derivados de 1,2,3-triazol pela cicloadição 1,3-dipolar de nitroalquenos com azida de sódio, sem a necessidade de catalisador e sob condições brandas.
Journal of the Brazilian Chemical Society. Publicado em: 2012-06
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22. A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações
The Copper-catalyzed azide-alkyne cycloaddition (CuAAC), often referred to as "click" reaction, has become a very popular reaction in the last years. It affords exclusively 1,4-disubstituted 1,2,3-triazoles and has been widely used to connect readily accessible building blocks containing various functional groups. The great success of this reaction is based
Química Nova. Publicado em: 2011
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23. Síntese de 1,2,3- triazóis ligados a 1,4- naftoquinona via reação de cicloadição 1,3- dipolar. / Synthesis of 1,2,3- triazoles connected 1,4-naphthoquinone via reation of 1,3-dipolar cycloaddition.
No presente trabalho foi realizada a síntese de uma nova série de derivados 1,2,3-triazólicos 1,4-dissubstituídos contendo o grupo naftoquinona na posição 1 deste anel heterocíclico a partir da reação de cicloadição 1,3-dipolar entre o precursor 2-azido-1,4-naftoquinona e 10 alcinos terminais, utilizando um método que emprega o uso de CuI como es
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 2011
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24. Synthesis and antimicrobial activity of chromone-linked 2-pyridone fused with 1,2,4-triazoles, 1,2,4-triazines and 1,2,4-triazepines ring systems
Três novas séries de sistemas heterocíclicos nitrogênio fundidos como o 1,2,4-triazol[1,5-α]piridinas (5-7 e 9), pirido[1,2-b][1,2,4]triazinas (10, 11, 13 e 15), e também pirido[1,2-b] [1,2,4]triazepinas (17, 18, 20 e 22) ligadas a um fragmento cromona foram sintetizadas a partir do intermediário-chave 1,6-diamino-(6-cloro-4-oxo-4H-chromen-3-il)-2-oxo
Journal of the Brazilian Chemical Society. Publicado em: 2010