Title of article :
An improved and versatile synthetic route to 6,7:13,14-dibenzo-1,8,4,11-dioxadiazacyclotetradecane
Author/Authors :
Mark Woods، نويسنده , , A.Dean Sherry، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
4
From page :
395
To page :
398
Abstract :
A new and effective synthetic pathway to 6,7:13,14-dibenzo-1,8,4,11-dioxadiazacyclotetradecane (1) has been developed. Beginning from salicylic acid, this synthetic pathway involves five high yielding steps to afford the macrocycle 6,7:13,14-dibenzo-1,8,4,11-dioxadiazacyclotetradecane-3,10-dione. Reduction of this macrocycle afforded the dioxadiaza crown 1 with an overall yield of 60%.
Keywords :
Azaoxacrownethers , Macrocyclic synthesis
Journal title :
INORGANICA CHIMICA ACTA
Serial Year :
2003
Journal title :
INORGANICA CHIMICA ACTA
Record number :
1321720
Link To Document :
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