Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Oct 1;15(19):2939-2951.
doi: 10.1002/asia.202000681. Epub 2020 Aug 28.

Construction of Axially Chiral Compounds via Central-to-Axial Chirality Conversion

Affiliations
Review

Construction of Axially Chiral Compounds via Central-to-Axial Chirality Conversion

Hui Yang et al. Chem Asian J. .

Abstract

Central-to-axial chirality conversion represents a fascinating class of chemical processes consisting of the destruction of stereogenic centers and the simultaneous installation of axial chiral elements, which provides efficient methods for the preparation of axially chiral compounds. Using the strategy, a wide range of axially chiral compounds, including biaryls, heterobiaryls, aromatic amides, allenes and vinyl arenes, have been synthesized with high efficiency and excellent enantioselectivity. In addition, central-to-axial chirality conversion strategy has been applied to the synthesis of natural products. The strategy has undoubtedly become and will continue to be a hot research topic in the field of asymmetric catalysis and synthesis. In this minireview, we selected some examples to introduce the developments and trends in the central-to-axial chirality conversion strategy up to April 2020.

Keywords: asymmetric catalysis; axially chiral; central-to-axial chirality conversion.

PubMed Disclaimer

Similar articles

Cited by

References

    1. F. Z. Abas, M. H. Uzir, M. H. M. Zahar, J. Applied Sci. 2010, 10, 3289-3294.
    1. E. Kumarasamy, R. Raghunathan, M. P. Sibi, J. Sivaguru, Chem. Rev. 2015, 115, 11239-11300.
    1. None
    1. M. C. Kozlowski, B. J. Morgan, E. C. Linton, Chem. Soc. Rev. 2009, 38, 3193-3207;
    1. G. Bringmann, T. Gulder, T. A. M. Gulder, M. Breuning, Chem. Rev. 2011, 111, 563-639.

LinkOut - more resources