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Synthesis of Chiral Flavanones from Tricarbonyl (η 6 -Arylbenzaldehyde)chromium(0)
Corresponding Author(s) : Hui Wu
wuhui72@yahoo.com.cn
Asian Journal of Chemistry,
Vol. 25 No. 14 (2013): Vol 25 Issue 14
Abstract
A synthesis of chiral flavanones via the condensation of tricarbonyl(h6-arylbenzaldehyde)chromium(0) and o-hydroxyacetophenone in a shorter time at room temperature have been developed. The tricarbonylchromium(0) group was removed by virtue of light and the enantioenriched flavanones was formed with highly enantioselectivity (> 95 % ee).
Keywords
Synthesis
Chiral flavanones
Chiral tricarbonylchromium(0) aromatic aldehydes
Liu, G.-X., Wan, Y., Zhao, L.-L., Wang, H.-Y., Xu, Z., Qi, J.-L., & Wu, H. (2013). Synthesis of Chiral Flavanones from Tricarbonyl (η 6 -Arylbenzaldehyde)chromium(0). Asian Journal of Chemistry, 25(14), 7828–7830. https://doi.org/10.14233/ajchem.2013.14634
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