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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-532618
- DOI to cite this document:
- 10.5283/epub.53261
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Abstract
A two-step protocol allowing the C−H amination of cyclic ethers with iminoiodinanes, followed by the reduction of the resulting intermediate has been developed for the preparation of amino alcohols. The initial C−H functionalization is accelerated by visible light, improving the reactivity compared to the thermal process performed in the dark. The effect of different substituents on the ...

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