Direct Catalytic Asymmetric Vinylogous Additions of α, β‐and β, γ‐Butenolides to Polyfluorinated Alkynyl Ketimines
Abstract We report a Zn‐ProPhenol catalyzed asymmetric Mannich reaction between
butenolides and polyfluorinated alkynyl ketimines to obtain vinylogous products featuring
two contiguous tetrasubstituted stereogenic centers. Notably, this is the first successful use
of ketimines in the ProPhenol Mannich process, and the reaction offers a new approach for
the preparation of pharmaceutically relevant products possessing trifluoromethylated
tetrasubstituted alkylamines. The reaction can be performed on large scale with reduced …
butenolides and polyfluorinated alkynyl ketimines to obtain vinylogous products featuring
two contiguous tetrasubstituted stereogenic centers. Notably, this is the first successful use
of ketimines in the ProPhenol Mannich process, and the reaction offers a new approach for
the preparation of pharmaceutically relevant products possessing trifluoromethylated
tetrasubstituted alkylamines. The reaction can be performed on large scale with reduced …
Abstract
We report a Zn‐ProPhenol catalyzed asymmetric Mannich reaction between butenolides and polyfluorinated alkynyl ketimines to obtain vinylogous products featuring two contiguous tetrasubstituted stereogenic centers. Notably, this is the first successful use of ketimines in the ProPhenol Mannich process, and the reaction offers a new approach for the preparation of pharmaceutically relevant products possessing trifluoromethylated tetrasubstituted alkylamines. The reaction can be performed on large scale with reduced catalyst loading without impacting its efficiency. Moreover, the acetylene moiety can be further elaborated using various methods.
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