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Efficient synthesis of 2-oxazolidinones and quinazoline-2,4(1 H ,3 H )-diones from CO 2 catalyzed by tetrabutylammonium fluoride

Tetrahedron, ISSN: 0040-4020, Vol: 74, Issue: 24, Page: 2914-2920
2018
  • 36
    Citations
  • 0
    Usage
  • 17
    Captures
  • 0
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    36
    • Citation Indexes
      36
  • Captures
    17

Article Description

By employing tetrabutylammonium fluoride (TBAF) as a catalyst, the various carboxylative cyclizations of the propargylic amines having internal alkynes with CO 2 proceeded to afford the corresponding 2-oxazolidinones. In this case, it was also found that the generated 2-oxazolidinones were tautomerized into the corresponding 2-oxazolones due to the basicity of TBAF. In addition, we performed the synthesis of quinazoline-2,4(1 H,3 H )-dione from 2-aminobenzonitrile and CO 2 by using TBAF as a catalyst.

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