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Enantioselective Total Synthesis of Aplyviolene

The enantioselective total synthesis of the rearranged spongian diterpene aplyviolene has been completed in 14 steps from the known hydroazulenone 8. The key junction of the hydrocarbon and oxygenated fragments to form the critical C8 quaternary carbon stereocenter and set the stage for elaborating...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Overman, Larry E., Schnermann, Martin J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3205941/
https://ncbi.nlm.nih.gov/pubmed/21936525
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja208018s
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