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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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Bibliografski detalji
Glavni autori: Hartung, John, Grubbs, Robert H.
Format: Artigo
Jezik:Inglês
Izdano: 2014
Teme:
Online pristup: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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