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Chiral Pentacarboxycyclopentadiene-Based Brønsted Acid-Catalyzed Enantioselective Desymmetrization of Meso-Epoxides by 2-Mercaptobenzothiazoles
[Image: see text] Enantioselective desymmetrization of meso-epoxides by 2-mercaptobenzothiazoles was realized by using the pentacarboxycyclopentadiene-based chiral Brønsted acid in combination of N-isopropylaniline as amine additive to give up to 90.5:9.5 er of the ring opening products.
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| Опубликовано в: : | ACS Omega |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
American Chemical Society
2018
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| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6644688/ https://ncbi.nlm.nih.gov/pubmed/31458851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsomega.8b01207 |
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