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- W2949285085 abstract "Abstract A new general synthetic route to obtain highly functionalized (Z)- and (E)-alk-1-enyl halides is described, where the halogen can be indistinctly F, Cl, Br, and I. The procedure involves CrCl2-promoted reductive elimination of β-O-substituted gem-dihalo alditols easily accessible from carbohydrates. The simplicity and mildness of the reaction conditions and their compatibility with different functional groups increase the synthetic potential of this methodology." @default.
- W2949285085 created "2019-06-27" @default.
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- W2949285085 date "2009-03-24" @default.
- W2949285085 modified "2023-09-23" @default.
- W2949285085 title "ChemInform Abstract: Chromium(II) Chloride-Promoted Reductive β-Elimination of 1,1-Dihalo Alditols. Synthesis of Highly Functionalized Alk-1-enyl Halides." @default.
- W2949285085 cites W2042999286 @default.
- W2949285085 doi "https://doi.org/10.1002/chin.200912191" @default.
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