Royal Society of Chemistry, Chemical Science, 8(11), p. 2121-2129, 2020
DOI: 10.1039/c9sc06089h
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A Mn porphyrin complex with a remote hydrogen bonding motif induces a high enantioselectivity in the oxygenation of 3-alkylquinolones. Compared to an achiral Mn complex, the site-selectivity was completely altered in favour of less reactive methylene groups.