Solid-phase synthesis of sulfamate peptidomimetics

被引:2
|
作者
Farrera-Sinfreu, Josep
Albericio, Fernando
Royo, Miriam
机构
[1] Univ Barcelona, Dept Organ Chem, E-08028 Barcelona, Spain
[2] Univ Barcelona, Combinatorial Chem Unit, E-08028 Barcelona, Spain
[3] Univ Barcelona, Inst Res Biomed, E-08028 Barcelona, Spain
来源
JOURNAL OF COMBINATORIAL CHEMISTRY | 2007年 / 9卷 / 03期
关键词
D O I
10.1021/cc070002g
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A synthetic method for the preparation of sulfamate peptidomimetics is described. The methodology allows sulfamoylation in the solid phase using sulfamoyl chloride in DMA, followed by the acylation of the corresponding sulfamoylated product. Following this approach, several derivatives have been prepared starting from distinct alcohol sources, including alpha-, beta-, and gamma-hydroxyacids and phenols. The presence of protected amino functions on the building blocks opens the possibility of the addition of more diversity. This approach, which is compatible with Fmoc/Boc/Alloc protection, provides a useful and efficient tool for the preparation of new sulfamate peptidomimetics.
引用
收藏
页码:501 / 506
页数:6
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