Catalytic Enantioselective Synthesis of Helicenes
- PMID: 36063162
- DOI: 10.1002/chem.202202369
Catalytic Enantioselective Synthesis of Helicenes
Abstract
Helicenes and helicene-like molecules, usually containing multiple ortho-fused aromatic rings, possess unique helical chirality. These compounds have found a wide range of important applications in many research fields, such as asymmetric catalysis, molecular recognition, sensors and responsive switches, circularly polarized luminescence materials and others. However, the catalytic enantioselective synthesis of helicenes was largely underexplored, when compared with the enantioselective synthesis of molecules bearing other stereogenic elements (e.g. central chirality and axial chirality). Since the pioneer work of asymmetric synthesis of helicenes via enantioselective [2+2+2] cycloaddition of triynes by Stará and Starý, last two decades have witnessed the tremendous development in the catalytic enantioselective synthesis of helicenes. In this review, we comprehensively summarized the advances in this field, which include methods enabled by both transition metal catalysis and organocatalysis, and provide our perspective on its future development.
Keywords: cyclization; enantioselective; helicenes; organocatalysis; transition metal catalysis.
© 2022 Wiley-VCH GmbH.
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References
-
- None
-
- C.-F. Chen, Y. Shen, Helicene Chemistry: From Synthesis to Applications, Berlin, Heidelberg: Springer Berlin/Heidelberg, Berlin, Heidelberg, 2016;
-
- Y. Shen, C.-F. Chen, Chem. Rev. 2012, 112, 1463-1535;
-
- M. Gingras, Chem. Soc. Rev. 2013, 42, 1051-1095;
-
- M. Gingras, Chem. Soc. Rev. 2013, 42, 968-1006;
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