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Direct synthesis of 1,5-disubstituted-4-magnesio-1,2,3-triazoles, revisited

Academic Article
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Overview

authors

  • Krasinski, A.
  • Fokin, Valery
  • Sharpless, K. Barry

publication date

  • April 2004

journal

  • Organic Letters  Journal

abstract

  • After revisiting earlier works reporting the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles via the addition of bromomagnesium acetylides to azides, much improved yields of the products were obtained for a wide array of azides and alkynes. The intermediates of that reaction can be trapped with different electrophiles to regioselectively form 1,4,5-trisubstituted 1,2,3-triazoles. [reaction: see text]

subject areas

  • Acetylene
  • Alkynes
  • Azides
  • Bromides
  • Chemistry, Pharmaceutical
  • Magnesium
  • Molecular Structure
  • Triazoles
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Identity

International Standard Serial Number (ISSN)

  • 1523-7060

Digital Object Identifier (DOI)

  • 10.1021/ol0499203

PubMed ID

  • 15070306
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Additional Document Info

start page

  • 1237

end page

  • 1240

volume

  • 6

issue

  • 8

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