2015
DOI: 10.1080/00397911.2015.1036452
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Chlorination of Calix[4]arene Derivatives

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(2 citation statements)
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“…In last decades, it has been seen that a well‐recognized direct C−H functionalization reactions [14] is a convenient way to introduce various functionalities into the upper rim of calixarene core in terms of atom‐economy / atom‐efficiency. Below in Table 1, we have shown the most typical examples of C−H functionalization of calix[4]arenes at the upper rim [15–26] …”
Section: Upper Rim Direct C‐h Functionalizationmentioning
confidence: 99%
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“…In last decades, it has been seen that a well‐recognized direct C−H functionalization reactions [14] is a convenient way to introduce various functionalities into the upper rim of calixarene core in terms of atom‐economy / atom‐efficiency. Below in Table 1, we have shown the most typical examples of C−H functionalization of calix[4]arenes at the upper rim [15–26] …”
Section: Upper Rim Direct C‐h Functionalizationmentioning
confidence: 99%
“…Below in Table 1, we have shown the most typical examples of CÀ H functionalization of calix [4]arenes at the upper rim. [15][16][17][18][19][20][21][22][23][24][25][26] Among the above reported derivatives (Table 1) in last two decades the para-sulfonato-calix [4]arenes (Table 1, entry 11) were found to possess highly diverse biomedical applications, [27] such as anti-HIV and anti-herpes activity, [28] antibacterial activity, [29] anti-thrombotic activities, [30] enzyme inhibiting activity, [31] ion-channel blocking activity, [32] and some other…”
Section: Direct C-h Functionalization At Para-positionmentioning
confidence: 99%