A bifunctional pyrazolone-chromone synthon directed organocatalytic double Michael cascade reaction: Forging five stereocenters in structurally diverse hexahydroxanthones

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ID: 64686
2019
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Abstract
An efficient method is reported to synthesize sulfonamides on DNA from sulfinic acids or sodium sulfinates and amines in the presence of iodine under mild conditions. This method demonstrates a major expansion of scope of sulfonamide formation on DNA through the utilization of a novel sodium carbonate-sodium sulfinate bifunctional reagent class.
Reference Key
liu2019aorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Liu, X.
Journal Organic Chemistry Frontiers
Year 2019
DOI
10.1039/c9qo00265k
URL
Keywords Keywords not found

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