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Synfacts 2010(4): 0473-0473
DOI: 10.1055/s-0029-1219518
DOI: 10.1055/s-0029-1219518
Organo- and Biocatalysis
© Georg Thieme Verlag
Stuttgart ˙ New York
Enantioselective Transfer Hydrogenation of Quinoxalines and Quinoxalinones
M. Rueping, F. Tato, F. R. Schoepke
RWTH Aachen, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
22. März 2010 (online)

Significance
Rueping and colleagues have shown that transfer hydrogenation catalyzed by BINOL-derived phosphoric acids of type 3 can be successfully applied to a variety of nitrogen heterocycles, including pyridines, quinolines, benzoxazines, benzthiazines, and benzoxazinones (see original publication for references). In this work, they disclose the hydrogenation of one further substrate class - quinoxalines 1 and quinoxalinones 2. Good to excellent yields and enantioselectivities were obtained with Hantzsch ester 4 and Brønsted acid 3 as the catalyst.