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Synthesis of fully substituted iminolactones via a three-component condensation of isocyanides and acetylenic esters with 2-bromo-1-(4-bromophenyl)ethanone

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Abstract

A novel three-component condensation reaction between an isocyanide, an electron-deficient acetylenic ester, and 2-bromo-1-(4-bromophenyl)‐ethanone efficiently provides fully substituted iminolactones in a one-pot condensation reaction without any activation or modification in high yields.

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Authors and Affiliations

  1. Department of Chemistry, Shahid Beheshti University, Tehran, Iran

    Ahmad Shaabani, Ebrohim Soleimani & Afshin Sarvary

Authors
  1. Ahmad Shaabani
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  2. Ebrohim Soleimani
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  3. Afshin Sarvary
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Corresponding author

Correspondence to Ahmad Shaabani.

Additional information

Correspondence: Ahmad Shaabani, Department of Chemistry, Shahid Beheshti University, P.O. Box 19396-4716, Tehran, Iran.

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Shaabani, A., Soleimani, E. & Sarvary, A. Synthesis of fully substituted iminolactones via a three-component condensation of isocyanides and acetylenic esters with 2-bromo-1-(4-bromophenyl)ethanone. Monatsh Chem 139, 629–632 (2008). https://doi.org/10.1007/s00706-007-0807-y

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  • DOI: https://doi.org/10.1007/s00706-007-0807-y

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