Ruthenium-catalyzed amino- and alkoxycarbonylations with carbamoylchlorides and alkyl chloroformates via aromatic C-H bond cleavage

Takuya Kochi, Seiya Urano, Hajime Seki, Eiichiro Mizushima, Mitsuo Sato, Fumitoshi Kakiuchi

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

(Figure Presented) Ruthenium-catalyzed regioselective direct amino- and alkoxycarbonylations of aromatic rings via C-H bond cleavage using chlorocarbonyl compounds are described. A broad generality of amide and ester groups was achieved taking advantage of the wide availability of carbonylating agents. Alkyl chloroformates, inapplicable to usual Friedel-Crafts methods, can also be used for direct catalytic alkoxycarbonylation.

Original languageEnglish
Pages (from-to)2792-2793
Number of pages2
JournalJournal of the American Chemical Society
Volume131
Issue number8
DOIs
Publication statusPublished - 2009 Mar 4

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ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Ruthenium-catalyzed amino- and alkoxycarbonylations with carbamoylchlorides and alkyl chloroformates via aromatic C-H bond cleavage. / Kochi, Takuya; Urano, Seiya; Seki, Hajime; Mizushima, Eiichiro; Sato, Mitsuo; Kakiuchi, Fumitoshi.

In: Journal of the American Chemical Society, Vol. 131, No. 8, 04.03.2009, p. 2792-2793.

Research output: Contribution to journalArticle

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AU - Sato, Mitsuo

AU - Kakiuchi, Fumitoshi

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