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Synthesis and reactivity of sulfamoyl azides and 1-sulfamoyl-1,2,3-triazoles

Academic Article
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Overview

authors

  • Culhane, J. C.
  • Fokin, Valery

publication date

  • September 2011

journal

  • Organic Letters  Journal

abstract

  • Sulfamoyl azides are readily generated from secondary amines and a novel sulfonyl azide transfer agent, 2,3-dimethyl-1H-imidazolium triflate. They react with alkynes in the presence of a CuTC catalyst forming 1-sulfamoyl-1,2,3-triazoles. The latter are shelf-stable progenitors of rhodium azavinyl carbenes, versatile reactive intermediates that, among other reactions, readily and asymmetrically add to olefins.

subject areas

  • Azides
  • Molecular Structure
  • Stereoisomerism
  • Triazoles
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Identity

PubMed Central ID

  • PMC3224852

International Standard Serial Number (ISSN)

  • 1523-7060

Digital Object Identifier (DOI)

  • 10.1021/ol201705k

PubMed ID

  • 21812453
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Additional Document Info

start page

  • 4578

end page

  • 4580

volume

  • 13

issue

  • 17

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