Lewis J E M, Bordoli R J, Denis M, Fletcher C J, Galli M, Neal E A, Rochette E M, Goldup S M
Chemistry , University of Southampton , Highfield , Southampton , SO17 1BJ , UK . Email:
School of Biological and Chemical Sciences , Queen Mary University of London , Mile End Road , London , E1 4NS , UK.
Chem Sci. 2016 May 1;7(5):3154-3161. doi: 10.1039/c6sc00011h. Epub 2016 Jan 27.
We present an operationally simple approach to 2,2'-bipyridine macrocycles. Our method uses simple starting materials to produce these previously hard to access rotaxane precursors in remarkable yields (typically >65%) across a range of scales (0.1-5 mmol). All of the macrocycles reported are efficiently converted (>90%) to rotaxanes under AT-CuAAC conditions. With the requisite macrocycles finally available in sufficient quantities, we further demonstrate their long term utility through the first gram-scale synthesis of an AT-CuAAC [2]rotaxane and extend this powerful methodology to produce novel Sauvage-type molecular shuttles.
我们提出了一种操作简便的合成2,2'-联吡啶大环化合物的方法。我们的方法使用简单的起始原料,在一系列规模(0.1 - 5 mmol)下以显著的产率(通常>65%)制备这些以前难以获得的轮烷前体。所报道的所有大环化合物在AT-CuAAC条件下都能高效转化(>90%)为轮烷。由于最终有足够数量的所需大环化合物,我们通过首次克级规模合成AT-CuAAC [2]轮烷进一步证明了它们的长期实用性,并扩展了这种强大的方法以制备新型的索瓦热型分子梭。