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Bioinspired Total Synthesis and Human Proteasome Inhibitory Activity of (−)-Salinosporamide A, (−)-Homosalinosporamide A, and Derivatives Obtained via Organonucleophile Promoted Bis-Cyclizations

A full account of concise, enantioselective syntheses of the anticancer agent (−)-salinosporamide A and derivatives, including (−)-homosalinosporamide, is described that was inspired by biosynthetic considerations. The brevity of the synthetic strategy stems from a key bis-cyclization of a (β)-keto...

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Dades bibliogràfiques
Publicat a:J Org Chem
Autors principals: Nguyen, Henry, Ma, Gil, Gladysheva, Tatiana, Fremgen, Trisha, Romo, Daniel
Format: Artigo
Idioma:Inglês
Publicat: 2010
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5546919/
https://ncbi.nlm.nih.gov/pubmed/21047113
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo101638r
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