Amino Imidate Catalyzed Asymmetric Michael Reactions of Ketones and Nitroalkenes
The efficiency of an amino imidate organocatalyst was evaluated in the Michael reaction of ketones with nitroalkenes. tert-Butyl l-proline imidate was found to be a syn-selective catalyst, generating products with moderate to good enantioselectivities of up to 84% ee. The best substrates were found...
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| Автори: | , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Georg Thieme Verlag KG
2022-02-01
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| Серія: | SynOpen |
| Предмети: | |
| Онлайн доступ: | http://www.thieme-connect.de/DOI/DOI?10.1055/a-1761-4495 |
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