Abstract
A palladium-catalyzed enantioselective three-component reaction of glyoxylic acid, sulfonamides and aryltrifluoroborates is described. This process provides modular access to the important α-arylglycine motif in moderate to good yields and enantioselectivies. The formed α-arylglycine products constitute useful building blocks for the synthesis of peptides or arylglycine-containing natural products.
Funder
Forschungsinitiative Rheinland-Pfalz
Cited by
2 articles.
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1. Catalytic multi-step domino and one-pot reactions;Beilstein Journal of Organic Chemistry;2024-02-08
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