Asymmetric Organocatalysis Under Mechanochemical Conditions

被引:6
|
作者
Nemethova, Viktoria [1 ]
Kristofikova, Dominika [1 ]
Meciarova, Maria [1 ]
Sebesta, Radovan [1 ]
机构
[1] Comenius Univ, Fac Nat Sci, Dept Organ Chem, Ilkovicova 6, Bratislava 84215, Slovakia
来源
CHEMICAL RECORD | 2023年 / 23卷 / 07期
关键词
asymmetric organocatalysis; mechanochemistry; covalent activation; non-covalent activation; ball-milling; SOLVENT-FREE; MICHAEL ADDITIONS; PHASE-TRANSFER; ALDOL REACTION; (S)-PROLINE-CONTAINING DIPEPTIDES; NITROALKENES; ACTIVATION; CATALYSIS; EFFICIENT; DERIVATIVES;
D O I
10.1002/tcr.202200283
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Asymmetric organocatalysis is a robust methodology providing access to numerous valuable compounds while having green chemistry principles in mind. The realization of organocatalytic transformation under solvent-free mechanochemical conditions brings additional benefits in terms of yields, selectivities, and, last but not least overall improved sustainability. This overview describes developments in the use of mechanochemistry as a vehicle for asymmetric organocatalytic transformations. The material is organized according to main catalytic activation modes, starting with covalent activation and proceeding to non-covalent activation modes. The advantages of mechanochemical organocatalytic reactions are particularly highlighted, but in some cases also, limitations are mentioned. Possibilities for target compound synthesis are also discussed.
引用
收藏
页数:13
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