Highly regioselective friedländer reaction

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

Research output: Contribution to journalArticlepeer-review

76 Scopus citations


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
Issue number8
StatePublished - Apr 19 2001
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry


Dive into the research topics of 'Highly regioselective friedländer reaction'. Together they form a unique fingerprint.

Cite this