Abstract
The chemoselective reduction of enamides to α-amino acids with iPrOH and EtOH as H-donors and solvents catalyzed by Ru pincer complexes is demonstrated. A range of α-amino acids is synthesized in good to excellent yields. Applications, large scale, and a one-pot experiment are also reported. Finally, deuterium-labeling experiments show high regioselectivity between the α- and β-positions of the alkene unit.
| Original language | English |
|---|---|
| Journal | Journal of organic chemistry |
| Volume | 87 |
| Issue number | 8 |
| Pages (from-to) | 5419-5423 |
| Number of pages | 5 |
| ISSN | 0022-3263 |
| DOIs | |
| Publication status | Published - 2022 |
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