期刊
CHEMICAL COMMUNICATIONS
卷 51, 期 12, 页码 2376-2379出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc09724f
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- SFI
- UCD School of Chemistry and Chemical Biology
Enantiopure C-2-symmetric iodoarenes based on the rigid all-carbon anti-dimethanoanthracene framework are shown to catalyse the asymmetric oxidative Kita spirolactonisation of propanoic acid-tethered 1-naphthols with significant levels of asymmetric induction of up to 67% ee.
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