C−N Axial Chiral Hypervalent Iodine Reagents: Catalytic Stereoselective α‐Oxytosylation of Ketones

A simple synthesis of a library of novel C−N axially chiral iodoarenes is achieved in a three‐step synthesis from commercially available aniline derivatives. C−N axial chiral iodine reagents are rarely investigated in the hypervalent iodine arena. The potential of the novel chiral iodoarenes as orga...

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Veröffentlicht in:Chemistry : a European journal 2021-03, Vol.27 (13), p.4317-4321
Hauptverfasser: Alharbi, Haifa, Elsherbini, Mohamed, Qurban, Jihan, Wirth, Thomas
Format: Artikel
Sprache:eng
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Zusammenfassung:A simple synthesis of a library of novel C−N axially chiral iodoarenes is achieved in a three‐step synthesis from commercially available aniline derivatives. C−N axial chiral iodine reagents are rarely investigated in the hypervalent iodine arena. The potential of the novel chiral iodoarenes as organocatalysts for stereoselective oxidative transformations is assessed using the well explored, but challenging stereoselective α‐oxytosylation of ketones. All investigated reagents catalyse the stereoselective oxidation of propiophenone to the corresponding chiral α‐oxytosylated products with good stereochemical control. Using the optimised reaction conditions a wide range of products was obtained in generally good to excellent yields and with good enantioselectivities. Novel C‐N axial chiral iodoarenes enable catalytic stereoselective α‐oxytosylations of ketones with high yields and improved enantioselectivities.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.202005253