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A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives promoted by Ca(OTf) 2

Tetrahedron Letters, ISSN: 0040-4039, Vol: 57, Issue: 19, Page: 2034-2038
2016
  • 8
    Citations
  • 0
    Usage
  • 11
    Captures
  • 0
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    8
    • Citation Indexes
      8
  • Captures
    11

Article Description

A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives has been reported using alkaline earth catalyst [Ca(OTf) 2 ]. Initially aryl amine reacts with ethyl propiolate to form β-enamino ester which further reacts with aryl aldehyde and indole in the presence of Ca(OTf) 2 to give indolyl acrylates. It is interesting to note that in the absence of indole the reaction leads to the formation of benzylidene bisacrylates. Similarly β-enamino ester reacts with another electrophilic partner isatin in the presence of Ca(OTf) 2 to give oxindolyl acrylates. The products were isolated in good yields by simple filtration.

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