Vicarious amination of nitroarenes with trimethylhydrazinium iodine

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Description

This paper investigated the use of 1,1,1-trimethylhydrazinium iodide as a vicarious nucleophilic substitution reagent for introducing amino groups into nitroaromatic substrates. The substrates included nitroarenes, polynitrobenzenes, picramide, TNB,TNT, and dinitropyrazole; other nitroazoles are being studied.

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13 p.

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Pagoria, P.F.; Schmidt, R.D. & Mitchell, A.R. November 10, 1995.

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Description

This paper investigated the use of 1,1,1-trimethylhydrazinium iodide as a vicarious nucleophilic substitution reagent for introducing amino groups into nitroaromatic substrates. The substrates included nitroarenes, polynitrobenzenes, picramide, TNB,TNT, and dinitropyrazole; other nitroazoles are being studied.

Physical Description

13 p.

Notes

OSTI as DE96009708

Source

  • Spring national meeting of the American Chemical Society (ACS), New Orleans, LA (United States), 24-28 Mar 1996

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  • Other: DE96009708
  • Report No.: UCRL-JC--122488
  • Report No.: CONF-960376--11
  • Grant Number: W-7405-ENG-48
  • Office of Scientific & Technical Information Report Number: 229365
  • Archival Resource Key: ark:/67531/metadc664106

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  • November 10, 1995

Added to The UNT Digital Library

  • June 29, 2015, 9:42 p.m.

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  • Feb. 18, 2016, 11:16 a.m.

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Pagoria, P.F.; Schmidt, R.D. & Mitchell, A.R. Vicarious amination of nitroarenes with trimethylhydrazinium iodine, article, November 10, 1995; California. (digital.library.unt.edu/ark:/67531/metadc664106/: accessed August 23, 2017), University of North Texas Libraries, Digital Library, digital.library.unt.edu; crediting UNT Libraries Government Documents Department.