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Titel:

Enantio- and Regioselective Epoxidation of Olefinic Double Bonds in Quinolones, Pyridones, and Amides Catalyzed by a Ruthenium Porphyrin Catalyst with a Hydrogen Bonding Site

Dokumenttyp:
Journal Article
Autor(en):
Fackler, P.; Huber, S. M.; Bach, T.
Abstract:
An array of differently substituted 3-alkenylquinolones was synthesized, and the enantio- and regioselectivity of their Ru-catalyzed epoxidation were studied. A precursor ruthenium(II) complex with a chiral tricyclic gamma-lactam skeleton (octahydro-1H-4,7-methanoisoindol-1-one) was available by Sonogashira cross-coupling with a monobromo-substituted ruthenium(II) porphyrin. Enantioselective epoxidation reactions (60-83
Kongresstitel:
ISI Document Delivery No.: 981CH Times Cited: 5 Cited Reference Count: 108 Fackler, Philipp Huber, Stefan M. Bach, Thorsten Huber, Stefan/F-7660-2011 Deutsche Forschungsgemeinschaft [Ba 1372-17]; TUM Graduate School; Fonds der Chemischen Industrie This project was supported by the Deutsche Forschungsgemeinschaft (Ba 1372-17) and by the TUM Graduate School. We thank Wacker-Chemie (Munich) for the donation of chemicals. S.M.H. thanks the Fonds der Chemischen Industrie for a Liebig fellowship. 5...     »
Zeitschriftentitel:
Journal of the American Chemical Society
Jahr:
2012
Band / Volume:
134
Heft / Issue:
30
Seitenangaben Beitrag:
12869-12878
Volltext / DOI:
doi:10.1021/ja305890c
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