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http://hdl.handle.net/10397/81223
Title: | Catalytic asymmetric oxo-Diels-Alder reactions with chiral atropisomeric biphenyl diols | Authors: | Yeung, CT Chan, WTK Lo, WS Law, GL Wong, WT |
Issue Date: | 2019 | Source: | Beilstein journal of nanotechnology, 2019, v. 15, p. 955-962 | Abstract: | New chiral atropisomeric biphenyl diols 3, 4 and 6 containing additional peripheral chiral centers with different steric bulkiness and/or electronic properties were synthesized. The X-ray crystal structure of 3 shows the formation of a supramolecular structure whereas that of 6, containing additional CF3 substituents, shows the formation of a monomeric structure. Diols 1-6 were found to be active organocatalysts in oxo-Diels-Alder reactions in which 2 recorded a 72% ee with trimethylacetaldehyde as a substrate. | Keywords: | Asymmetric organocatalysis Axial chirality Biaryls Hydrogen bond Oxo-Diels-Alder reaction |
Publisher: | Beilstein-Institut Zur Forderung der Chemischen Wissenschaften | Journal: | Beilstein journal of nanotechnology | EISSN: | 1860-5397 | DOI: | 10.3762/bjoc.15.92 | Rights: | © 2019 Yeung et al. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The following publication Yeung, C.-T.; Chan, W. T. K.; Lo, W.-S.; Law, G.-L.; Wong, W.-T. Beilstein J. Org. Chem. 2019, 15, 955–962 is available at https://doi.org/10.3762/bjoc.15.92 |
Appears in Collections: | Journal/Magazine Article |
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