Catalytic enantioselective Friedlaender condensations: Facile access to quinolines with remote stereogenic centers
Enamine catalysis enables the first catalytic enantioselective Friedlaender reaction. The desymmetrization of 4-substituted cyclohexanones upon reaction with o-aminobenzaldehydes allows for the synthesis of quinolines with remote stereogenic centers. Thes
Li, Le,Seidel, Daniel
supporting information; experimental part
p. 5064 - 5067
(2010/12/25)
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