Title of article
A versatile strategy for the synthesis of crown ether-bearing heterocycles: Discovery of calcium-selective fluoroionophore Original Research Article
Author/Authors
Yuko Aoki، نويسنده , , Naoki Umezawa، نويسنده , , Yuko Asano، نويسنده , , Keiichiro Hatano، نويسنده , , Yuki Yano، نويسنده , , Nobuki Kato، نويسنده , , Tsunehiko Higuchi، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
8
From page
7108
To page
7115
Abstract
Heterocycles have been modified in various ways in the search for new functions, but few examples are known of crown ethers incorporating heterocycles in macro-ring systems. Here we report a simple and versatile synthesis of crown ether-bearing heterocycles. An acylurea moiety in the heterocycles is efficiently transformed to ‘crown ether’ of various ring sizes. The products included a Ca2+-selective fluoroionophore. Our simple methodology is expected to provide many novel functional heterocyclic compounds, including fluoroionophores and candidate pharmaceuticals.
Keywords
calcium , Magnesium , Crown ether , Coordination , Fluoroionophore , One-step synthesis , Acylurea , Metal sensor , Uracil , Lumazine , Cesium effect , fluorescence , Lumichrome , Phenytoin , Phenobarbital , crystal structure , Heterocycle , Selectivity
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2007
Journal title
Bioorganic and Medicinal Chemistry
Record number
1303801
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