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- W2952361091 abstract "The chromium Reformatsky reaction allows the highly chemoselective addition of ester enolates to aldehydes or methyl ketones at room temperature. Aldehyde selectivities of ≥ 50:1 vs. methyl ketones and ≥ 200:1 vs. larger ketones and other electrophiles can be achieved in most cases. Methyl ketones are preferred with similar effectivity against higher ketones. Effects of solvents, lithium iodide and substituents are discussed." @default.
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- W2952361091 title "Excellent Aldehyde and Ketone Selectivity in Chromium(II)-Mediated Reformatsky Reactions" @default.
- W2952361091 doi "https://doi.org/10.1055/s-1997-3239" @default.
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