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Amplification of anti-Diastereoselectivity via Curtin-Hammett Effects in Ruthenium Catalyzed Hydrohydroxyalkylation of 1,1-Disubstituted Allenes: Diastereoselective Formation of All-Carbon Quaternary Centers

Under the conditions of ruthenium catalyzed transfer hydrogenation, 1,1-disubstituted allenes 1a–1c and alcohols 2a–2g engage in redox-triggered generation of allylruthenium-aldehyde pairs to form products of hydrohydroxyalkylation 3a–3g, 4a–4g and 5a–5g with complete branched regioselectivity. By e...

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Bibliografiset tiedot
Päätekijät: Zbieg, Jason R., McInturff, Emma L., Leung, Joyce C., Krische, Michael J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2010
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3030639/
https://ncbi.nlm.nih.gov/pubmed/21175178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja1104156
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