Metal-free visible-light-enabled vicinal trifluoromethyl dithiolation of unactivated alkenes
Submitting author affiliation: Nanjing University, Nanjing, China
Beilstein Arch. 2021, 20211. https://doi.org/10.3762/bxiv.2021.1.v1
Published 13 Jan 2021
Read the peer-reviewed version of this preprint: https://doi.org/10.3762/bjoc.17.49
Abstract
The difunctionalization of alkenes involving trifluoromethylthio group (SCF3) for the conversion of versatile and readily available olefins into more structurally complex molecules has been greatly studied. However, the disproportionate dithiolation of alkene is unknown. Herein, a transition-metal-free protocol is presented for vicinal trifluoromethylthio-thiolation of unactivated alkenes via a radical process under mild condition with broad substrate scope and excellent tolerance.
Keywords: metal-free, photoredox, difunctionalization, trifluoromethylthiolation, alkenes.
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When a peer-reviewed version of this preprint is available, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:
Li, X.; Zhang, Q.; Zhang, W.; Ma, J.; Wang, Y.; Pan, Y. Beilstein Arch. 2021, 20211. doi:10.3762/bxiv.2021.1.v1
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