Convenient one-step Synthesis of Substituted Pyrano[2,3-c]isoquinoline (2-amino-4H-chromenes) via three Component Reaction between Alkyl isocyanides and Dialkyl Acetylenedicarboxylate in the presence of 3-Hydroxyisoquinoline

Authors

  • Bita Mohtat Karaj Branch, Islamic Azad University, Karaj
  • Shahla Salmani Karaj Branch, Islamic Azad University, Karaj
  • Amineh Aminian Karaj Branch, Islamic Azad University, Karaj
  • Hoorieh Djahaniani East Tehtan Branch, Islamic Azad University, Tehran

DOI:

https://doi.org/10.24297/jac.v6i1.966

Keywords:

4H-chromenes, alkyl isocyanides, acetylenic ester, 3-hydroxyisoquinoline

Abstract

The reactive intermediate generated by the addition of alkyl isocyanides to dialkyl acetylenedicarboxylate are trapped by 3-hydroxyisoquinoline to produce highly functionalized 4H-chromenes in 83-92% yields.

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Author Biographies

  • Bita Mohtat, Karaj Branch, Islamic Azad University, Karaj
    Chemistry Department
  • Shahla Salmani, Karaj Branch, Islamic Azad University, Karaj
    Chemistry Department
  • Amineh Aminian, Karaj Branch, Islamic Azad University, Karaj
    Chemistry Department
  • Hoorieh Djahaniani, East Tehtan Branch, Islamic Azad University, Tehran
    Chemistry Department

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Published

2010-04-10

Issue

Vol. 6 No. 1 (2013)

Section

Articles

License

Creative Commons License All articles published in Journal of Advances in Linguistics are licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

Convenient one-step Synthesis of Substituted Pyrano[2,3-c]isoquinoline (2-amino-4H-chromenes) via three Component Reaction between Alkyl isocyanides and Dialkyl Acetylenedicarboxylate in the presence of 3-Hydroxyisoquinoline. (2010). JOURNAL OF ADVANCES IN CHEMISTRY, 6(1), 873-877. https://doi.org/10.24297/jac.v6i1.966

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