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Título

Synthesis of New Statin Derivatives

AutorChioua, Mourad CSIC ORCID ; Marco-Contelles, José CSIC ORCID
Palabras claveHeterocycles
Michaelreaction
Nitrones
Statins
Synthetic Methods
Fecha de publicación2021
EditorChemPubSoc Europe
CitaciónChemistrySelect 6: 13633- 13635 (2021)
ResumenHerein we report the synthesis of the new statin derivative MC609 in 80 % overall yield by sequential transformation of simvastatin including dehydration, and Michael addition of N-benzyl hydroxylamine followed by cyclization. The preparation of nitronestatins MC649 and MC645 is also described from (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-6-oxotetrahydro-2H-pyran-2-carbaldehyde by reaction with N-benzyl hydroxylamine, and N-hydroxylamine followed by reduction with sodium cyanoborohydride and coupling with commercially available 2-chloro-6-methylquinoline-3-carbaldehyde, in 77 % and 24 % overall yield, respectively.
Versión del editorhttp://dx.doi.org/10.1002/slct.202103544
URIhttp://hdl.handle.net/10261/260868
DOI10.1002/slct.202103544
Identificadoresdoi: 10.1002/slct.202103544
issn: 2365-6549
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