Rhenium-catalyzed diastereoselective synthesis of aminoindanes via the insertion of allenes into a C-H bond

Yoichiro Kuninobu, Peng Yu, Kazuhiko Takai

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

Figure Presented. Aminoindane derivatives were synthesized diastereoselectively by the treatment of aromatic imines with allenes in the presence of a catalytic amount of a rhenium complex, [HRe(CO)4] n. The allenes inserted into the aromatic C-H bonds.

Original languageEnglish
Pages (from-to)4274-4276
Number of pages3
JournalOrganic Letters
Volume12
Issue number19
DOIs
Publication statusPublished - Oct 1 2010

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Rhenium-catalyzed diastereoselective synthesis of aminoindanes via the insertion of allenes into a C-H bond'. Together they form a unique fingerprint.

  • Cite this