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  Sulfoxide-mediated Umpolung of alkali halide salts

Klimczyk, S., Huang, X., Farès, C., & Maulide, N. (2012). Sulfoxide-mediated Umpolung of alkali halide salts. Organic & Biomolecular Chemistry, 10(22), 4327-4329. doi:10.1039/C2OB25459J.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-CA2F-B Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-CA30-5
Genre: Journal Article

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c2ob25459j.pdf (Supplementary material), 878KB
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https://hdl.handle.net/11858/00-001M-0000-0014-CA31-3
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2012
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The Royal Society of Chemistry
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 Creators:
Klimczyk, Sebastian1, Author           
Huang, Xueliang1, Author           
Farès, Christophe2, Author           
Maulide, Nuno1, Author           
Affiliations:
1Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445614              
2Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445623              

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 Abstract: A new protocol for the direct two-electron oxidative Umpolung of alkali halide salts is reported. This procedure, relying on the use of a commercially available sulfoxide as the oxidant, allows the electrophilic halogenation of carbonyl compounds as well as halolactonisation reactions to proceed from the corresponding sodium salts, at room temperature and under mild conditions.

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Language(s): eng - English
 Dates: 2012-03-012012-03-122012-04-032012-06-14
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/C2OB25459J
 Degree: -

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Title: Organic & Biomolecular Chemistry
  Other : Organic and Biomolecular Chemistry
  Abbreviation : Org. Biomol. Chem.
Source Genre: Journal
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Publ. Info: Cambridge : Royal Society of Chemistry
Pages: 3 Volume / Issue: 10 (22) Sequence Number: - Start / End Page: 4327 - 4329 Identifier: ISSN: 1477-0520
CoNE: https://pure.mpg.de/cone/journals/resource/954925269322