| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269317 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The sequential reaction including alcohol oxidation by TEMPO/Cu system and the asymmetric aldol reaction by peptide catalysis was realized using resin-supported catalysts. The step of oxidizing primary alcohols to the corresponding aldehydes could be dramatically enhanced through the introduction of triglycyl peptide to supported TEMPO and the method of pre-adsorbing a Cu-complex into resin beads.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kengo Akagawa, Shota Takigawa, Erika Mano, Kazuaki Kudo,