REGIOSELECTIVE SYNTHESIS OF 1,7-DIPROTECTED 1,4,7,10-TETRAAZACYCLODODECANE AND PREPARATION OF A DIALCOHOL DICARBOXYLIC MACROCYCLIC LIGAND

被引:46
作者
DUMONT, A [1 ]
JACQUES, V [1 ]
PENG, QX [1 ]
DESREUX, JF [1 ]
机构
[1] UNIV LIEGE,B-4000 SART,BELGIUM
关键词
D O I
10.1016/S0040-4039(00)73077-2
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of 1,4,7,10-tetraazacyclododecane with p-toluenesulfonyl chloride in pyridine or with diethyl phosphite and CCl4 in a water/CH2Cl2 mixture yields selectively the 1,7-diprotected regioisomer. The 1,7-diprotected tetraaza cycles are interesting starting materials, for instance for the preparation of 4,10-bis(2'-hydroxyethyl)-1,7-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane.
引用
收藏
页码:3707 / 3710
页数:4
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