| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5289235 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Acetophenone reacted with a series of aromatic aldehydes with grinding under catalysis of a double-component solid base system consisting of NaOH and K2CO3 to furnish highly chemoselectively 1,2,3,4,5-pentasubstituted cyclohexanols in 80-95% yield, and their composition and structure are identified by spectral technologies and single crystal X-ray diffraction analysis, and a possible mechanism of the formation was suggested.
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Authors
Xinxiang Luo, Zixing Shan,