High yielding synthesis of 2,2′-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes

被引:71
作者
Lewis, J. E. M. [1 ]
Bordoli, R. J. [2 ]
Denis, M. [1 ]
Fletcher, C. J. [1 ]
Galli, M. [1 ]
Neal, E. A. [2 ]
Rochette, E. M. [1 ]
Goldup, S. M. [1 ]
机构
[1] Univ Southampton, Chem, Southampton SO17 1BJ, Hants, England
[2] Queen Mary Univ London, Sch Biol & Chem Sci, Mile End Rd, London E1 4NS, England
基金
英国工程与自然科学研究理事会;
关键词
ACTIVE-TEMPLATE SYNTHESIS; SWITCHABLE MOLECULAR SHUTTLES; PHOTOPHYSICAL PROPERTIES; ARYL HALIDES; POLYAMINE MACROCYCLES; DIRECTED SYNTHESIS; CRYSTAL-STRUCTURE; TERMINAL ALKYNES; EFFICIENT METHOD; LIGANDS;
D O I
10.1039/c6sc00011h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:3154 / 3161
页数:8
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