In the presence of a peptide catalyst and the oxidative enzyme laccase, a one-pot sequential reaction including a Friedel-Crafts-type alkylation of α,β-unsaturated aldehydes followed by an α-oxyamination was realized. The reaction in aqueous solvent to promote the enzymatic oxidation, and the use of a peptide catalyst compatible with such conditions, were essential. The present sequential reaction afforded oxygen-functionalized indole or pyrrole derivatives in a highly enantioselective manner. © 2012 Akagawa et al; licensee Beilstein-Institut. License and terms: see end of document.
CITATION STYLE
Akagawa, K., Umezawa, R., & Kudo, K. (2012). Asymmetric one-pot sequential Friedel-Crafts-type alkylation and α-oxyamination catalyzed by a peptide and an enzyme. Beilstein Journal of Organic Chemistry, 8, 1333–1337. https://doi.org/10.3762/bjoc.8.152
Mendeley helps you to discover research relevant for your work.