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Novel and efficient one-pot five- and six-component reactions for the stereoselective synthesis of highly functionalized enaminones and dithiocarbamates

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Abstract

Efficient methods for stereoselective synthesis of polyfunctional (E)-enaminones and (Z)-dithiocarbamates via one-pot five- and six-component sequential Ugi/Nucleophilic addition reactions are described. High yields and high bond forming efficiency, and simple operations are the advantages of this method.

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Authors and Affiliations

  1. Peptide Chemistry Research Group, K. N. Toosi University of Technology, P.O. Box 15875-4416, Tehran, Iran

    Morteza Bararjanian, Saeed Balalaie & Barahman Movassagh

  2. Organisch-Chemisches Institut der Universitaet Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany

    Frank Rominger

  3. Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran

    Hamid Reza Bijanzadeh

Authors
  1. Morteza Bararjanian
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  2. Saeed Balalaie
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  3. Frank Rominger
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  4. Barahman Movassagh
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  5. Hamid Reza Bijanzadeh
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Corresponding author

Correspondence to Saeed Balalaie.

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Dedicated to Prof. Nasser Iranpoor on the occasion of his 55th Birthday.

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Bararjanian, M., Balalaie, S., Rominger, F. et al. Novel and efficient one-pot five- and six-component reactions for the stereoselective synthesis of highly functionalized enaminones and dithiocarbamates. Mol Divers 15, 583–594 (2011). https://doi.org/10.1007/s11030-010-9286-x

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  • DOI: https://doi.org/10.1007/s11030-010-9286-x

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