The stereochemical course of 2-methylisoborneol biosynthesis
Both enantiomers of 2-methyllinalyl diphosphate (2-Me-LPP) were synthesized enantioselectively using Sharpless epoxidation as a key step and purification of enantiomerically enriched intermediates through HPLC separation on a chiral stationary phase. Their enzymatic conversion with 2-methylisoborneo...
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Beilstein-Institut
2022-07-01
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| Schriftenreihe: | Beilstein Journal of Organic Chemistry |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.3762/bjoc.18.82 |
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