Clayden Jonathan
School of Chemistry, University of Manchester, Oxford Rd., Manchester, UK M13 9PL.
Chem Soc Rev. 2009 Mar;38(3):817-29. doi: 10.1039/b801639a. Epub 2008 Dec 8.
By exploiting intramolecular interactions such as dipole repulsion, and by incorporating a terminal chiral controlling feature, the global conformation of a molecule may be governed. In such an environment, stereoselective reactions can occur at considerable distances from the source of stereochemical information, providing a simple method for information relay over scales of >1 nm (or about seven bond lengths). This tutorial review discusses the development of this idea, and describes examples which depend on relayed dipole repulsion and on the absolute control of helicity. Future prospects in the area employing control over extended helical foldamers are elaborated.
通过利用分子内相互作用(如偶极排斥),并引入末端手性控制特征,可以控制分子的整体构象。在这样的环境中,立体选择性反应可以在距立体化学信息源相当远的距离处发生,从而提供了一种在大于1纳米(或约七个键长)的尺度上进行信息传递的简单方法。本教程综述讨论了这一概念的发展,并描述了依赖于传递偶极排斥和螺旋度绝对控制的实例。阐述了在利用对扩展螺旋折叠体的控制方面该领域的未来前景。