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Microwave-assisted synthesis of biologically relevant steroidal 17-exo-pyrazol-5'-ones from a norpregnene precursor by a side-chain elongation/heterocyclization sequence

Multistep syntheses of novel 17β-pyrazol-5'-ones in the Δ(5)-androstane series were efficiently carried out from pregnenolone acetate. A steroidal 17-carboxylic acid was first synthesized as a norpregnene precursor by the bromoform reaction and subsequent acetylation. Its CDI-activated acylimid...

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Detalles Bibliográficos
Publicado en:Beilstein J Org Chem
Main Authors: Mótyán, Gergő, Mérai, László, Kiss, Márton Attila, Schelz, Zsuzsanna, Sinka, Izabella, Zupkó, István, Frank, Éva
Formato: Artigo
Idioma:Inglês
Publicado: Beilstein-Institut 2018
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6204839/
https://ncbi.nlm.nih.gov/pubmed/30410620
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.14.236
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