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- W3159122811 endingPage "10246" @default.
- W3159122811 startingPage "10226" @default.
- W3159122811 abstract "Catalyst-controlled functionalization of unmodified carbonyl compounds is a relevant operation in organic synthesis, especially when high levels of site- and stereoselectivity can be attained. This objective is now within reach for some subsets of enolizable substrates using various types of activation mechanisms. Recent contributions to this area include enantioselective transformations that proceed via transiently generated noncovalent di(tri)enolate-catalyst coordination species. While relatively easier to form than simple enolate congeners, di(tri)enolates are ambifunctional in nature and so control of the reaction regioselectivity becomes an issue. This Minireview discusses in some detail this and other problems, and how noncovalent activation approaches based on metallic and metal free catalysts have been developed to advance the field." @default.
- W3159122811 created "2021-05-10" @default.
- W3159122811 creator A5075479167 @default.
- W3159122811 creator A5081374328 @default.
- W3159122811 date "2021-06-10" @default.
- W3159122811 modified "2023-10-14" @default.
- W3159122811 title "Extended Enolates: Versatile Intermediates for Asymmetric C‐H Functionalization via Noncovalent Catalysis" @default.
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