Manganese-catalyzed cleavage of a carbon-carbon single bond between carbonyl carbon and α-carbon atoms of ketones

Yoichiro Kuninobu, Tadamasa Uesugi, Atsushi Kawata, Kazuhiko Takai

Research output: Contribution to journalArticle

55 Citations (Scopus)

Abstract

Singled out: Treatment of ketones with carbodiimides in the presence of a catalytic amount of either [{HMn(CO)4}3] or [Mn 2(CO)10] gave amides in good to excellent yields. In this reaction, the carbon-carbon single bond of a ketone is cleaved efficiently. The reaction also proceeded by using isocyanates instead of carbodiimides.

Original languageEnglish
Pages (from-to)10406-10408
Number of pages3
JournalAngewandte Chemie - International Edition
Volume50
Issue number44
DOIs
Publication statusPublished - Oct 24 2011

Fingerprint

Carbodiimides
Carbon Monoxide
Manganese
Ketones
Carbon
Isocyanates
Atoms
Amides
single bond

Keywords

  • C-C cleavage
  • ketone
  • manganese
  • reaction mechanisms
  • synthetic methods

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis

Cite this

Manganese-catalyzed cleavage of a carbon-carbon single bond between carbonyl carbon and α-carbon atoms of ketones. / Kuninobu, Yoichiro; Uesugi, Tadamasa; Kawata, Atsushi; Takai, Kazuhiko.

In: Angewandte Chemie - International Edition, Vol. 50, No. 44, 24.10.2011, p. 10406-10408.

Research output: Contribution to journalArticle

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