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Highly Catalytic Enantioselective Reformatsky Reaction with Aldehydes and Ketones Using an Available Prolinol Ligand
[Image: see text] A highly Me(2)Zn-mediated catalytic enantioselective Reformatsky reaction of aldehydes and ketones with ethyl iodoacetate using a readily available prolinol ligand is reported. This reaction provides an efficient method for the construction of β-hydroxy esters in up to 98% yield an...
Tallennettuna:
| Julkaisussa: | ACS Omega |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Chemical Society
2020
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| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7366354/ https://ncbi.nlm.nih.gov/pubmed/32685867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsomega.0c02400 |
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