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Download fileAsymmetric Synthesis of Spiropyrazolones via Chiral Pd(0)/Ligand Complex-Catalyzed Formal [4+2] Cycloaddition of Vinyl Benzoxazinanones with Alkylidene Pyrazolones
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posted on 2020-12-30, 20:07 authored by Jia-Ming Guo, Xiao-Zu Fan, Hui-Hui Wu, Zhe Tang, Xiao-Fan Bi, Heng Zhang, Lu-Yu Cai, Hong-Wu Zhao, Qi-Di ZhongIn
the presence of the chiral Pd(0)/ligand complex, vinyl benzoxazinanones
underwent the [4+2] cycloaddition with alkylidene pyrazolones smoothly
and delivered spiropyrazolones in reasonable yields, diastereoselectivities,
and eneantioselectivities (up to >99% yield, >99:1 dr and 99%
ee).
The absolute configuration of the obtained spiropyrazolones was unambiguously
characterized with the use of X-ray single-crystal structure analysis.
Moreover, the reaction mechanism was assumed to interpret the formation
of the target compounds.
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presenceeePdspiropyrazolonecycloadditionComplex-CatalyzeddrdiastereoselectivitieAlkylidene Pyrazolonesalkylidene pyrazolonesVinyl BenzoxazinanonesFormalAsymmetric SynthesisChiralformationX-ray single-crystal structure analysisconfigurationSpiropyrazolonechiraltarget compoundsreaction mechanismyieldeneantioselectivitievinyl benzoxazinanonesCycloaddition