Strain Release Chemistry of Photogenerated Small-Ring Intermediates

被引:27
|
作者
Luque, Adriana [1 ]
Paternoga, Jan [1 ]
Opatz, Till [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
关键词
green chemistry; photochemistry; ring strain; strain-release; transition-metal catalysis; PYRIDINIUM SALT PHOTOCHEMISTRY; RETRO-MANNICH FRAGMENTATION; INTRAMOLECULAR PHOTOCYCLOADDITION; CYCLOBUTANE DERIVATIVES; PHOTOREDOX CATALYSIS; NATURAL-PRODUCTS; AB-INITIO; LIGHT; CYCLIZATION; STEREOCHEMISTRY;
D O I
10.1002/chem.202004178
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photochemical processes, such as isomerizations and cycloadditions, have proven to be very useful in the construction of highly strained molecular frameworks. Photoinduced ring strain enables subsequent exergonic reactions which do not require the input of additional chemical energy and provides a variety of attractive synthetic options leading to complex structures. This review covers the progress achieved in the application of sequences combining excitation by ultraviolet light to form strained intermediates, which are further transformed to lower energy products in strain-release reactions. As ring strain is considerable in small ring systems, photogenerated three- and four-membered rings will be covered, mainly focusing on examples from 2000 to May 2020.
引用
收藏
页码:4500 / 4516
页数:17
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