2015
DOI: 10.18083/lcappl.2015.3.52
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Mesomorphic Esters of 4-Alkyl(aryl)cyclohexenecarboxylic Acids. Synthesis and Properties

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Cited by 2 publications
(4 citation statements)
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“…Previously we have demonstrated that [3 + 2] 1,3-dipolar cycloaddition of arylnitrile oxide to alkene is a excellent route to access different 3,5-disubstituted isoxazolines (Tavares et al, 2010(Tavares et al, , 2016Fritsch & Merlo, 2016;Lopes et al, 2018). Using this methodology, a collection of isoxazolines can be constructed with specific applications ranging from biological compounds through use as intermediates in organic synthesis to liquid-crystal materials (El-Khatatneh et al, 2017;Fader & Carreira, 2004;Bezborodov et al, 2004). With this purpose in mind, we have established a concise route to the synthesis of liquid crystals based on isoxazolines and their full characterization.…”
Section: Chemical Contextmentioning
confidence: 99%
“…Previously we have demonstrated that [3 + 2] 1,3-dipolar cycloaddition of arylnitrile oxide to alkene is a excellent route to access different 3,5-disubstituted isoxazolines (Tavares et al, 2010(Tavares et al, , 2016Fritsch & Merlo, 2016;Lopes et al, 2018). Using this methodology, a collection of isoxazolines can be constructed with specific applications ranging from biological compounds through use as intermediates in organic synthesis to liquid-crystal materials (El-Khatatneh et al, 2017;Fader & Carreira, 2004;Bezborodov et al, 2004). With this purpose in mind, we have established a concise route to the synthesis of liquid crystals based on isoxazolines and their full characterization.…”
Section: Chemical Contextmentioning
confidence: 99%
“…The 3,6-disubstituted cyclohex-2-enones (I) with different combinations of cyclic, bridge, terminal fragments and lateral substituents can be prepared in a high yield and in a "one pot procedure" by the condensation of the corresponding Mannich salts or 2-chloro(bromo)ethylaryl(alkyl)ketones with 2-substituted acetoacetic esters, 4-substituted methylbenzylketones or other β-dicarbonylic compounds in the presence of potassium hydroxide in a boiling dioxane [23]. The following catalytic hydrogenation of the cyclohex-2-enones (I) in the presence of 10% palladium on charcoal and potassium hydroxide in isopropanol or THF-isopropanol mixture leads to the appropriate trans-2,5-disubstituted cyclohexanones (II) (Scheme 1).…”
Section: Synthesis Of the Intermediatesmentioning
confidence: 99%
“…Derivatives of terphenyls and quaterphenyl(18)(19)(20)(21)(22)(23)(24)(25).Scheme 7. Preparation of LC compounds(26,(28)(29)(30) …”
mentioning
confidence: 99%
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