2017
DOI: 10.1016/j.bmcl.2016.12.074
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Synthesis and cell imaging applications of fluorescent mono/di/tri-heterocyclyl-2,6-dicyanoanilines

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Cited by 9 publications
(8 citation statements)
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“…26,27 With the aldehyde group an attractive handle for synthetic diversification, such compounds have also served as synthons for preparing bioimaging, 28 anti-cancer, 23,24 and antituberculosis 26,27 agents. Likewise, 4-imino-1,2,3-triazoles formed from amine condensation reactions have been shown to be useful for constructing novel coordination compounds.…”
mentioning
confidence: 99%
“…26,27 With the aldehyde group an attractive handle for synthetic diversification, such compounds have also served as synthons for preparing bioimaging, 28 anti-cancer, 23,24 and antituberculosis 26,27 agents. Likewise, 4-imino-1,2,3-triazoles formed from amine condensation reactions have been shown to be useful for constructing novel coordination compounds.…”
mentioning
confidence: 99%
“…4-Formyl-1,2,3-triazoles, also known as 1,2,3-triazole-4-carbaldehydes, are widely present in the literature, mainly due to the synthetic versatility of the formyl group [1][2][3][4][5][6][7]. In the field of medicinal chemistry [7], triazole-4-carbaldehydes have been prepared as intermediates in the synthesis of anticancer [8][9][10], antifungal [11,12], antituberculosis [13][14][15], anti-inflammatory [10,16], antidiabetic [17], and even bioimaging agents [18]. Furthermore, imine derivatives have been synthesized as interesting ligands in coordination chemistry [19][20][21].…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, imine derivatives have been synthesized as interesting ligands in coordination chemistry [19][20][21]. 1-Substituted 4-formyl-1,2,3-triazoles are commonly prepared via a two-step synthesis involving the copper-catalyzed azide-alkyne cycloaddition reaction with azides and propargyl alcohol [2,[9][10][11][12][13][15][16][17][18]22] or acetal-protected propargyl aldehydes [3,5,6,8,23,24], followed by oxidation or hydrolysis, respectively. These methods are clever alternatives for the cycloaddition between azides and the low boiling propynal, which is inconvenient to handle.…”
Section: Introductionmentioning
confidence: 99%
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“…2,6‐Dicyanoanilines are useful intermediates for organic synthesis . They also have been used as optical materials and cell image agents . The reported synthetic methods for 2,6‐dicyanoanilines include i) three‐component reactions of aldehydes, ketones and malononitrile; ii) reactions of chalcones with malononitrile in guanidinium ionic liquids; iii) three‐component reactions of α,β‐unsaturated imines with malononitrile; iv) reactions of aldehydes, β‐nitroolefins and malononitrile catalyzed by DMAP; v) reactions of 1,3‐diketones with three equiv.…”
Section: Introductionmentioning
confidence: 99%