Highly regioselective friedländer reaction

Yi Hsiao, Nelo R. Rivera, Nobuyoshi Yasuda, David L. Hughes, Paul J. Reider

Research output: Contribution to journalArticle

71 Scopus citations

Abstract

Matrix presented A highly regioselective Friedländer reaction is described. By introduction of a phosphonate group at one of the α-carbons of a ketone, regioselectivity can be perfectly controlled.

Original languageEnglish (US)
Pages (from-to)1101-1103
Number of pages3
JournalOrganic letters
Volume3
Issue number8
DOIs
StatePublished - Apr 19 2001
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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  • Cite this

    Hsiao, Y., Rivera, N. R., Yasuda, N., Hughes, D. L., & Reider, P. J. (2001). Highly regioselective friedländer reaction. Organic letters, 3(8), 1101-1103. https://doi.org/10.1021/ol006785v