4.8 Article

Chiral β-iodoamines by urea-catalysed iodocyclization of trichloroacetimidates

期刊

CHEMICAL SCIENCE
卷 4, 期 5, 页码 2100-2104

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3sc50410g

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  1. NIGMS CMLD program [P50GM069721]
  2. American Cancer Society
  3. NSERC

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Highly enantioselective vicinal iodoamination of olefins is accomplished through the iodocyclization of alkenyl trichloroacetimidates catalysed by a new chiral Schiff-base urea derivative. The resulting products are converted readily to a variety of polyfunctional amine-containing chiral building blocks.

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