Issue 71, 2022

Site-selective C–H alkylation of myo-inositol via organic photoredox catalysis

Abstract

Site-selective photoredox reactions with aromatic olefins enable direct alkylation of unprotected myo-inositol at C4. The efficacy of these reactions can be finely tuned by modifying the structures of HAT reagents. These reactions open the possibility of selective C–H alkylations of myo-inositol without the need for multi-step protection–deprotection strategies.

Graphical abstract: Site-selective C–H alkylation of myo-inositol via organic photoredox catalysis

Supplementary files

Article information

Article type
Communication
Submitted
11 Jul 2022
Accepted
05 Aug 2022
First published
10 Aug 2022

Chem. Commun., 2022,58, 9934-9937

Site-selective C–H alkylation of myo-inositol via organic photoredox catalysis

H. Cao, T. Guo, X. Deng, X. Huo, S. Tang, J. Liu and X. Wang, Chem. Commun., 2022, 58, 9934 DOI: 10.1039/D2CC03569C

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