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Enantioselective Diamination with Novel Chiral Hypervalent Iodine Catalysts

118

Citations

47

References

2014

Year

Abstract

Abstract Vicinal diamines constitute one the most important functional motif in organic chemistry because of its wide occurrence in a variety of biological and pharmaceutical molecules. We report an efficient metal‐free, highly stereoselective intramolecular diamination using a novel chiral hypervalent iodine reagent together with its application as an efficient catalyst for the synthesis of diamines.

References

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