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Synfacts 2011(6): 0624-0624
DOI: 10.1055/s-0030-1260388
DOI: 10.1055/s-0030-1260388
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of 2,3-Disubstituted Indolines by Asymmetric Hydrogenation
D.-S. Wang, J. Tang, Y.-G. Zhou*, M.-W. Chen, C.-B. Yu, Y. Duan, G.-F. Jiang*
Dalian Institute of Chemical Physics and Hunan University, Changsha, P. R. of China
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
19. Mai 2011 (online)

Significance
Asymmetric hydrogenation of heterocycles is a challenging transformation due to the need to destroy aromaticity. The authors have previously developed a method for activating unprotected indoles for hydrogenation (J. Am. Chem. Soc. 2010, 132, 8909). In the present report, they utilize 3-(α-hydroxyalkyl)indoles, which can be activated by dehydration, allowing for a highly enantioselective palladium-catalyzed hydrogenation to take place.