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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| Main Authors: | , , , , , |
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| Format: | Book |
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Georg Thieme Verlag KG,
2021-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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