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KHMDS enhanced SmI(2)-mediated reformatsky type alpha-cyanation.

Ankner, Tobias, 1976 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Fridén-Saxin, Maria, 1979 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Pemberton, Nils, 1978 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
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Seifert, Tina, 1985 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Grøtli, Morten, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Luthman, Kristina, 1953 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Hilmersson, Göran, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
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 (creator_code:org_t)
2010-04-29
2010
English.
In: Organic letters. - : American Chemical Society (ACS). - 1523-7052 .- 1523-7060. ; 12:10, s. 2210-3
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A novel combination of SmI(2), KHMDS, and TsCN can be utilized to introduce a cyano group into structurally diverse and highly sensitive 2-alkyl-chroman-4-ones. Subsequent oxidation allows the formed 2-alkyl-3-cyanochromones to be isolated in yields ranging from 49 to 77%. In addition, alpha-bromoketones and esters were found to undergo equally effective alpha-cyanation.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

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