2006
DOI: 10.1016/j.tet.2006.03.095
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Microwave-assisted synthesis of calix[4]resorcinarenes

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Cited by 42 publications
(38 citation statements)
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“…Excellent isolated yields (up to 90%) were attained within short reaction times (typically, 3-5 min) when the reaction was performed under microwaves irradiation (Scheme 25) [73].…”
Section: Synthesis Of Calix[4]resorcinarenesmentioning
confidence: 99%
“…Excellent isolated yields (up to 90%) were attained within short reaction times (typically, 3-5 min) when the reaction was performed under microwaves irradiation (Scheme 25) [73].…”
Section: Synthesis Of Calix[4]resorcinarenesmentioning
confidence: 99%
“…Calix [4]resorcinarenes [1] are analogs of calixarene having two hydroxy groups on benzene rings at extra annular position forming a macrocycle. Calix [4]resorcinarenes are synthesized by the acid-catalyzed cyclocondensation of resorcinol with various aliphatic or aromatic aldehydes [2][3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…Calix [4]resorcinarenes are synthesized by the acid-catalyzed cyclocondensation of resorcinol with various aliphatic or aromatic aldehydes [2][3][4][5]. They have found application as macrocyclic receptor [6], as dendrimers in biological systems [7][8][9], nano-capsule [10], nanoparticales [11,12], opticalchemosensors [13], supramolecular tectons [14][15][16], host molecules [17,18], as components in liquid crystals [19,20], photo resists [21][22][23], selective membranes [24,25], surface reforming agents [26], HPLC stationary phase [27], as ion channel mimics [28], and metal ion extraction agents [29][30][31].…”
Section: Introductionmentioning
confidence: 99%
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