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.
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页数:13
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