Add time:07/11/2019 Source:sciencedirect.com
The photoisomerization of α-(9″-anthryl)ethyl spiro[cyclopropane-1,9′-fluorene]-2-carboxylates (1c⇄2c) proceeds diastereoselectively through the selective intramolecular energy transfer from the second triplet state of anthryl group to the fluorenyl moiety. Asymmetric induction using optically active α-(9″-anthryl)ethyl group is achieved in high optical and chemical yields.
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