The study demonstrates Evans’ (R)-4-benzyl-2-oxazolidinone auxiliary enables efficient asymmetric synthesis of finerenone, achieving stereoselective naphthyridine core construction with 86:14 dr and 80% yield. Subsequent ammonia-mediated transami...
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Selective Synthesis of Furan‐3(2H)‐one Fused Seven‐, Eight‐, or Nine‐Membered Ring from the Reaction of Diynone and Cyclic β‐Keto Ester
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A domino reaction of diynone and cyclic β-keto ester has been disclosed. This reaction provides a new strategy for the synthesis of a series of furan-3(2H)-one fused seven-, eight-, or nine-membered ring with good stereoselectivity and atom economy. Mechanistically, this reaction involves sequential Michael addition, intramolecular cyclization, ring opening, isomerization, anti-Michael addition and protonation.
A domino reaction of diynone and cyclic β-keto ester has been disclosed. This reaction provides a new strategy for the synthesis of a series of furan-3(2H)-one fused seven-, eight-, or nine-membered ring with good stereoselectivity and atom economy.
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