REGIOSELECTIVE SYNTHESIS OF CALIXCROWNS DERIVED FROM P-TERT-BUTYLCALIX[5]ARENE

被引:53
作者
KRAFT, D [1 ]
ARNECKE, R [1 ]
BOHMER, V [1 ]
VOGT, W [1 ]
机构
[1] UNIV MAINZ,INST ORGAN CHEM,JJ BECHER WEG 34 SB1,W-6500 MAINZ,GERMANY
关键词
D O I
10.1016/S0040-4020(01)87186-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Alkylation of p-tert-butylcalix[5]arene with oligoethylene glycol-ditosylates in the presence of CsF affords the 1,3-bridged calix[5]crowns la-c in 51 to 72% yield. In the case of hexaethylene glycol the isomeric 1,2-bridged calix[5]crown-7 2c was obtained additionally. The calixcrowns were further modified by alkylation of the remaining hydroxyl groups.
引用
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页码:6019 / 6024
页数:6
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