Stereoselective Total Syntheses of (3,5)-Sonnerlactone and (3,5)-Sonnerlactone
A highly convergent and concise total syntheses of (3 R ,5 R )-Sonnerlactone and (3 R ,5 S ) Sonnerlactone from a readily available L -malic acid is described. The following series of reactions such as Barbier allylation, photochemical esterification and Ring Closing Metathesis (RCM) are utilized as...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
SAGE Publishing
2017-09-01
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| Serie: | Natural Product Communications |
| Accesso online: | https://doi.org/10.1177/1934578X1701200925 |
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