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pro vyhledávání: '"Matthias Kähny"'
Publikováno v:
Angewandte Chemie International Edition. 53:13780-13784
A rhodium-catalyzed chemo-, regio-, and enantioselective addition of 2-pyridones to terminal allenes to give branched N-allyl 2-pyridones is reported. Preliminary mechanistic studies support the hypothesis that the reaction was initiated from the mor
Autor:
Matthias Kähny, Antje Meißner, Dietmar A. Plattner, Urs Gellrich, Alberto Steffani, Hans-Joachim Drexler, Bernhard Breit, Detlef Heller
Publikováno v:
Journal of the American Chemical Society. 136:1097-1104
Previously we reported the redox-neutral atom economic rhodium catalyzed coupling of terminal alkynes with carboxylic acids using the DPEphos ligand. We herein present a thorough mechanistic investigation applying various spectroscopic and spectromet
Publikováno v:
Journal of the American Chemical Society. 137(8)
We report on the first enantioselective variant of the atom-economic and redox-neutral coupling of carboxylic acids with terminal alkynes under rhodium catalysis utilizing the chiral, bidentate (R,R)-Cp-DIOP ligand. This represents the first example