2016
DOI: 10.3390/molecules21030307
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Synthesis of Isoxazole and 1,2,3-Triazole Isoindole Derivatives via Silver- and Copper-Catalyzed 1,3-Dipolar Cycloaddition Reaction

Abstract: Abstract:The CuI-or Ag 2 CO 3 -catalyzed [3+2] cycloaddition of propargyl-substituted dihydroisoindolin-1-one (3) with arylnitrile oxides 1a-d (Ar = Ph, p-MeC 6 H 4 , p-MeOC 6 H 4 , p-ClC 6 H 4 ) produces in good yields novel 3,5-disubstituted isoxazoles 4 of the ethyl-2-benzyl-3-oxo-1-((3-arylisoxazol-5yl)methyl)-2,3-dihydro-1H-isoindole-1-carboxylate type. With aryl azides 2a-d (Ar = Ph, p-MeC 6 H 4 , p-OMeC 6 H 4 , p-ClC 6 H 4 ), a series of 1,4-disubstituted 1,2,3-triazoles 6 (ethyl-2-benzyl-3-oxo-1-((1-ar… Show more

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Cited by 13 publications
(12 citation statements)
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“…On the other hand, the 1 H NMR spectrum of 5a displays the resonance of the isoxazole proton as a singlet at δ = 6.49 ppm. This chemical shift is in line with the values reported by Fokin and Sharpless and our previous work . In the case of reverse regioisomers, isoxazole proton should resonate at a chemical shift higher than 6.5 ppm because of the proximity of the isoxazolinic oxygen atom particularly characteristic are the 13 C NMR isoxazole ring resonances with three peaks at δ = 101.2, 162.7, and 166.0 ppm, in accordance with the data reported by Fokin and Sharpless …”
Section: Resultssupporting
confidence: 92%
“…On the other hand, the 1 H NMR spectrum of 5a displays the resonance of the isoxazole proton as a singlet at δ = 6.49 ppm. This chemical shift is in line with the values reported by Fokin and Sharpless and our previous work . In the case of reverse regioisomers, isoxazole proton should resonate at a chemical shift higher than 6.5 ppm because of the proximity of the isoxazolinic oxygen atom particularly characteristic are the 13 C NMR isoxazole ring resonances with three peaks at δ = 101.2, 162.7, and 166.0 ppm, in accordance with the data reported by Fokin and Sharpless …”
Section: Resultssupporting
confidence: 92%
“…Both these moieties have physicochemical and pharmacokinetic similarities and individually have been integrated at the place of ethylene bridge for cis configuration rigidification of CA‐4 (compound 6 & 8 , Figure ). Earlier reported synthetic derivatives of CA‐4 also had retained the original anti‐tubulin target specificity . The isoxazoline and 1, 2, 3‐ triazole are enriched with lone pair of electrons along with pi electrons in the double bonds which impart non‐covalent interactions.…”
Section: Introductionmentioning
confidence: 97%
“…Earlier reported synthetic derivatives of CA-4 also had retained the original anti-tubulin target specificity. [22][23][24][25][26][27][28][29][30][31][32][33][34][35] The isoxazoline and 1, 2, 3-triazole are enriched with lone pair of electrons along with pi electrons in the double bonds which impart noncovalent interactions. Both moieties show biological potential with a plethora of pharmacological effects on varying connecting molecular-skeletal combinations.…”
Section: Introductionmentioning
confidence: 99%
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“…Silver and copper are reported as catalysts, in a new and efficient way, for the cycloaddition of propargyl-substituted dihydroisoindolin-1-one with arylnitrile oxides to produce novel 3,5-disubstituted isoxazoles of the ethyl-2-benzyl-3-oxo-1-((3-arylisoxazol-5yl)methyl)-2,3-dihydro-1H-isoindole-1-carboxylate type [2]. Yields are significantly improved with the presence of Cu I as catalyst compared to the uncatalyzed reaction, without changing the selectivity.…”
mentioning
confidence: 99%