Skip to content
2000
Volume 5, Issue 3
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A concise formal synthesis of (±)-shikonin via a highly α-regioselective prenylation is achieved. The novelty of the procedure lies in the introduction of side chain of shikonin in one step via prenylation of 1, 4, 5, 8- tetramethoxynaphthalene-2-carbaldehyde under mild conditions without producing any γ-isomer.

Loading

Article metrics loading...

/content/journals/loc/10.2174/157017808783955899
2008-04-01
2025-10-30
Loading full text...

Full text loading...

/content/journals/loc/10.2174/157017808783955899
Loading

  • Article Type:
    Research Article
Keyword(s): oxonia-cope rearrangement; prenylation; regioselectivity; Shikonin; synthesis
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test