Maity Prantik, König Burkhard
Institut für Organische Chemie, Universität Regensburg, D-93040 Regensburg, Germany.
Org Lett. 2008 Apr 3;10(7):1473-6. doi: 10.1021/ol8002749. Epub 2008 Mar 12.
The terphenyl structure has been proven to be an ideal scaffold mimicking side-chain functionalities of peptidic alpha-helices. The synthesis of 1,4-dipiperazino benzenes, using stepwise transition metal-catalyzed N-arylation of chiral piperazines to a central benzene core is reported. The structure determination by X-ray crystallography reveals a geometrical arrangement of the hydrophobic side chains resembling the orientation of key i, i + 3, and i + 7 positions in a peptidic alpha-helix or in terphenyl helix mimetics.
三联苯结构已被证明是一种理想的支架,可模拟肽类α-螺旋的侧链功能。本文报道了通过逐步过渡金属催化手性哌嗪与中心苯核的N-芳基化反应合成1,4-二哌嗪基苯。X射线晶体学确定的结构揭示了疏水侧链的几何排列,类似于肽类α-螺旋或三联苯螺旋模拟物中关键的i、i + 3和i + 7位置的取向。