2008
DOI: 10.1002/jhet.5570450341
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Synthesis and liquid crystalline properties of novel pyridine derivatives

Abstract: The treatment of 4‐hydroxypyridine with cholestery p‐(ω‐bromoalkyloxy)benzoates in N,N‐dimethylformamide containing K2CO3 gave cholestery p‐[ω‐(4‐pyridyloxy)alkyloxy]benzoates, which exhibited liquid crystalline properties

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Cited by 9 publications
(2 citation statements)
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“…It is worth mentioning that 4-hydroxypyridine is a very appealing starting material as it can be either N-or O-alkylated in the first step [4][5][6], yielding either 4-pyridones or O-substituted pyridines respectively, followed by a second alkylation step to yield desired ILC materials. This represents a big advantage as different mesogenic groups can be introduced separately in the molecule with the aim of finely tune the liquid crystalline properties.…”
Section: Introductionmentioning
confidence: 99%
“…It is worth mentioning that 4-hydroxypyridine is a very appealing starting material as it can be either N-or O-alkylated in the first step [4][5][6], yielding either 4-pyridones or O-substituted pyridines respectively, followed by a second alkylation step to yield desired ILC materials. This represents a big advantage as different mesogenic groups can be introduced separately in the molecule with the aim of finely tune the liquid crystalline properties.…”
Section: Introductionmentioning
confidence: 99%
“…Numerous previous reports indicated that the 4-hydroxypyridine precursors could be either N - or O -alkylated with various halide compounds giving either N -alkylated 4-pyridones or O -substituted pyridines, respectively [ 24 , 36 , 37 , 38 , 39 ].…”
Section: Resultsmentioning
confidence: 99%