Enantioselective Strategies for The Synthesis of N-N Atropisomers

被引:40
作者
Centonze, Giovanni [1 ,2 ]
Portolani, Chiara [1 ,2 ]
Righi, Paolo [1 ,2 ]
Bencivenni, Giorgio [1 ,2 ]
机构
[1] Alma Mater Studiorum Univ Bologna, Dept Ind Chem Toso Montanari, Viale Risorgimento 4, I-40136 Bologna, Italy
[2] Alma Mater Studiorum Univ Bologna, Ctr Chem Catalysis C3, Viale Risorgimento 4, I-40136 Bologna, Italy
关键词
Alkylation; Hydrazides; Indoles; N-N Atropisomers; Pyrroles; CATALYTIC ASYMMETRIC-SYNTHESIS; ALDOL CONDENSATION SYNTHESIS; ATROPOSELECTIVE SYNTHESIS; AXIAL CHIRALITY; RESOLUTION; ANILIDES; ALLYLATION; ARYLATION; INDOLES; BIARYLS;
D O I
10.1002/anie.202303966
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Axially chiral compounds have been always considered a laboratory curiosity with rare prospects of being applied in asymmetric synthesis. Things have changed very quickly in the last twenty years when it was understood the important role and the enormous impact that these compounds have in medicinal, biological and material chemistry. The asymmetric synthesis of atropisomers became a rapidly expanding field and recent reports on the development of N-N atropisomers strongly prove how this research field is a hot topic open to new challenges and frontiers of asymmetric synthesis. This review focuses on the recent advances in the enantioselective synthesis of N-N atropisomers highlighting the strategies and breakthroughs to obtain this novel and stimulating atropisomeric framework.
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页数:15
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