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Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic α-Chlorination of Aldehydes
[Image: see text] The enantioselective aminocatalytic α-chlorination of aldehydes is a challenging reaction because of its tendency to proceed through neutral intermediates in unselective pathways. Herein we report the rational shift to a highly selective reaction pathway involving charged intermedi...
Tallennettuna:
| Julkaisussa: | J Am Chem Soc |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Chemical
Society
2021
|
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8297727/ https://ncbi.nlm.nih.gov/pubmed/33929823 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.1c02997 |
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