Synlett 2015; 26(06): 839-845
DOI: 10.1055/s-0034-1380124
letter
© Georg Thieme Verlag Stuttgart · New York

Synthesis and Selenation of Tandem Multicomponent Condensation Adducts

Authors

  • Guoxiong Hua

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • Junyi Du

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • Amy L. Fuller

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • Kasun S. A. Arachchige

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • David B. Cordes

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • Alexandra M. Z. Slawin

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
  • J. Derek Woollins*

    EaStCHEM School of Chemistry, University of St Andrews, Fife, KY16 9ST, UK   Email: jdw3@st-and.ac.uk
Further Information

Publication History

Received: 10 November 2014

Accepted after revision: 23 December 2014

Publication Date:
03 February 2015 (online)


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Abstract

A number of four-component condensation adducts, which were readily obtained from one-pot reaction of aryl carboxylic acids, arylaldehydes, arylamines, and c-hexylisocyanide, were treated with two equivalents of Woollins’ reagent leading to the formation of a series of novel selenoamides with one or two C=Se groups or heterocyclic compounds such as 1,3-selenazole and 1,3-selenazolidin-5-one.

Supporting Information