Selective beta-oxidation of alpha-sulfanyl amides

Typeset version

 

TY  - JOUR
  - Kissane, Marie and Murphy, Maureen and Bateman, Lorraine M. and McCarthy, Daniel G. and Maguire, Anita R.
  - 2011
  - Tetrahedron
  - Selective beta-oxidation of alpha-sulfanyl amides
  - Validated
  - ()
  - 67
  - 30
  - 5494
  - 5499
  - A selective beta-oxidation of a series of alpha-sulfanyl amides to the corresponding beta-oxo-alpha-sulfanyl amides is described. This selective efficient oxidation of an unfunctionalised methyl or methylene group occurs under mild conditions, involving three sequential transformations conducted without isolation of the intermediates. Critically neither the sulfur nor the reactive alpha-CH bond is affected in the overall process. (C) 2011 Elsevier Ltd. All rights reserved.
  - 10.1016/j.tet.2011.05.041
DA  - 2011/NaN
ER  - 
@article{V119669218,
   = {Kissane, Marie and Murphy, Maureen and Bateman, Lorraine M. and McCarthy, Daniel G. and Maguire, Anita R.},
   = {2011},
   = {Tetrahedron},
   = {Selective beta-oxidation of alpha-sulfanyl amides},
   = {Validated},
   = {()},
   = {67},
   = {30},
  pages = {5494--5499},
   = {{A selective beta-oxidation of a series of alpha-sulfanyl amides to the corresponding beta-oxo-alpha-sulfanyl amides is described. This selective efficient oxidation of an unfunctionalised methyl or methylene group occurs under mild conditions, involving three sequential transformations conducted without isolation of the intermediates. Critically neither the sulfur nor the reactive alpha-CH bond is affected in the overall process. (C) 2011 Elsevier Ltd. All rights reserved.}},
   = {10.1016/j.tet.2011.05.041},
  source = {IRIS}
}
AUTHORSKissane, Marie and Murphy, Maureen and Bateman, Lorraine M. and McCarthy, Daniel G. and Maguire, Anita R.
YEAR2011
MONTH
JOURNAL_CODETetrahedron
TITLESelective beta-oxidation of alpha-sulfanyl amides
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME67
ISSUE30
START_PAGE5494
END_PAGE5499
ABSTRACTA selective beta-oxidation of a series of alpha-sulfanyl amides to the corresponding beta-oxo-alpha-sulfanyl amides is described. This selective efficient oxidation of an unfunctionalised methyl or methylene group occurs under mild conditions, involving three sequential transformations conducted without isolation of the intermediates. Critically neither the sulfur nor the reactive alpha-CH bond is affected in the overall process. (C) 2011 Elsevier Ltd. All rights reserved.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINK10.1016/j.tet.2011.05.041
FUNDING_BODY
GRANT_DETAILS