4.5 Article

Catalytic Enantioselective α-Oxysulfonylation of Ketones Mediated by Iodoarenes

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2008, 期 31, 页码 5315-5328

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200800741

关键词

Hypervalent iodine reagents; Organocatalysis; Oxidation; Stereoselective synthesis

资金

  1. Cardiff University and the Royal Society of Chemistry (RSC)
  2. Engineering and Physical Sciences Research Council (EPSRC)
  3. National Mass Spectrometry Service Centre, Swansea
  4. Michigan State University Mass Spectrometry Services
  5. EPSRC
  6. US National Science Foundation [INT-0209956]
  7. Albion College

向作者/读者索取更多资源

The alpha-oxysulfonylation of ketones catalysed by enantio enriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity. We believe this to be the first report of an enantioselective organocatalytic reaction involving hypervalent iodine reagents which should open up a new field for enantioselective organocatalysis of oxidation reactions. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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