Asymmetric Synthesis of 1,2-Limonene Epoxides by Jacobsen Epoxidation
Abstract This study reported an asymmetric synthesis of 1,2-limonene epoxides. The absolute stereochemistry was controlled by a Jacobsen epoxidation of cis-1,2-limonene epoxide (with diastereomeric excess of 98%) and trans-1,2-limonene epoxide (with diastereomeric excess of 94%), which could be used...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Georg Thieme Verlag KG
2021-09-01
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| Serier: | Pharmaceutical Fronts |
| Fag: | |
| Online adgang: | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0041-1740241 |
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