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Catalytic, Enantioselective Synthesis of 1,2-anti Diols via Asymmetric Ring Opening/Cross Metathesis
An enantioselective method for the synthesis of 1,2-anti diols has been developed. A cyclometallated chiral-at-Ru complex catalyzes the asymmetric ring opening/cross metathesis of di–oxygenated cyclobutenes, resulting in functionally rich synthetic building blocks. Syntheses of the insect pheromone...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4037230/ https://ncbi.nlm.nih.gov/pubmed/24554613 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201310767 |
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