
Journal of Organic Chemistry p. 754 - 757 (1994)
Update date:2022-08-25
Topics:
Yeh, Mei-ling
Tang, Fa-shin
Chen, Shu-ling
Liu, Wen-chin
Lin, Lee-gin
The p-arylazo-substituted calix<4>arenes were synthesized by a diazo-coupling reaction between calix<4>arene and the diazonium salt of 6-amino-1,3-benzodioxin.The monoarylazo-, 1,2-diarylazo-, 1,3-diarylazo-, triarylazo-, and tetraarylazo-para-substituted calix<4>arenes were isolated and characterized by spectral methods. 6-Amino-1,3-benzodioxin was prepared by palladium metal reduction of 6-nitro-1,3-benzodioxin.
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