Skip to content
2000
Volume 13, Issue 3
  • ISSN: 1573-4064
  • E-ISSN: 1875-6638

Abstract

Background: Biaryl seven-membered lactones (BSLs), the target compounds are a class of bioactive compounds with anti-arrhythmic activity, which also serve as a starting material or structural units for chemical synthesis. Objective: To report a simple and efficient procedure for the synthesis of biaryl seven-membered lactones. Method: Under microwave, the umpolung reaction was promoted by N-heterocyclic carbenes under oxygen, with anhydrous potassium carbonate as base and with 1,4,7,10,13,16-Hexanoxacyclooctadecane (18-crown-6) as a phase-transfer catalyst. Results: The practical protocol was found to be compatible with different structurally diverse substrates and with moderate to excellent yields. Conclusion: This synthesis method has the advantage of high efficacy and novelty, short reaction time, operation simplicity, mild condition and high yields, providing a useful and atom-economic approach to the synthesis of BSLs.

Loading

Article metrics loading...

/content/journals/mc/10.2174/1573406413666161117121441
2017-05-01
2025-05-24
Loading full text...

Full text loading...

/content/journals/mc/10.2174/1573406413666161117121441
Loading

  • Article Type:
    Research Article
Keyword(s): BSLs; carbene salt; lactones; microwave; N-heterocyclic carbine; umpolung reaction
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