Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
197016 | Electrochimica Acta | 2005 | 10 Pages |
Abstract
Efficient asymmetric carbon–carbon bond-forming reaction at the 2-position of a piperidine skeleton was achieved through scrutinizing chiral catalysts, copper ions, nucleophiles, and reaction temperatures. The key intermediates in this method were 2-methoxy-3,4-didehydropiperidines, which were easily prepared by electrochemical oxidation of 1-protected piperidines in methanol followed by didehydrogenation of the oxidation products. This method involved a chiral Cu(II) catalyzed coupling reaction between 1-(4-methoxybenzoyl)-3,4-didehydro-2-methoxypiperidine and nucleophiles such as dimethyl malonate and methyl acetoacetate to afford 2-substituted piperidines with up to 82%e.e. (e.e., enantiomeric excess).
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Osamu Onomura, Yasuhisa Kanda, Mieko Imai, Yoshihiro Matsumura,