| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269590 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
A simple catalytic, redox-neutral access to 3-methylcyclohexenones has been developed via rhodium catalysis in the presence of an amine additive and Ag2CO3. This process utilized simple aldehydes and acetone as substrates and tolerates a variety of functional groups. Disubstituted phenols were isolated in moderate yields when Cu(OAc)2 was employed as an oxidant.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Fen Wang, Yuchen Liu, Zisong Qi, Wei Dai, Xingwei Li,