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Construction of a Spirooxindole Amide Library through Nitrile Hydrozirconation-Acylation-Cyclization Cascade

A library of spirooxindoles containing varied elements of structural and stereochemical diversity has been constructed via a three step, one pot nitrile hydrozirconation-acylation-cyclization reaction sequence from common acyclic indole intermediates. The resulting library was evaluated for novelty...

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Bibliografiset tiedot
Päätekijät: LaPorte, Matthew G., Tsegay, Sammi, Hong, Ki Bum, Lu, Chunliang, Fang, Cheng, Wang, Lirong, Xie, Xiang-Qun, Floreancig, Paul E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3800499/
https://ncbi.nlm.nih.gov/pubmed/23731121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/co4000387
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