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• Click chemistry
  '''Click chemistry''', for which [[K. Barry Sharpless]] won the [[Nobel Prize]] in [[Chemistry Most substituted triazoles are synthesized by one of several click chemistry methods. One method uses [[palladium]] (Pd) catalysts to couple [[alkyne|al
  3 KB (437 words) - 14:16, 6 February 2010
• Click chemistry/Definition
  141 bytes (18 words) - 13:06, 6 February 2010
• Click chemistry/Related Articles
  337 bytes (50 words) - 13:09, 6 February 2010
• Click chemistry/External Links
  [http://www.scripps.edu/chem/sharpless/click.html Over 900 click chemistry citations at www.scripps.edu/chem/sharpless/click.html]
  143 bytes (21 words) - 13:12, 6 February 2010

Page text matches

• Click chemistry/External Links
  [http://www.scripps.edu/chem/sharpless/click.html Over 900 click chemistry citations at www.scripps.edu/chem/sharpless/click.html]
  143 bytes (21 words) - 13:12, 6 February 2010
• Tetrazole/External Links
  [http://www.scripps.edu/chem/sharpless/click.html Over 900 click chemistry citations at www.scripps.edu/chem/sharpless/click.html]
  143 bytes (21 words) - 14:39, 6 February 2010
• Tetrazole
  ...d one carbon atom form a 5-atom heterocycle. They can be synthesized by [[click chemistry]], reacting a [[cyanide]] with an [[azide]], as depicted below. The base t {{Image|Tetrazole Click chemistry.png|right|350px|Tetrazole formed by cyclization of a cyanide and an azide.}
  672 bytes (100 words) - 14:38, 6 February 2010
• Tetrazole/Related Articles
  {{r|Click chemistry}}
  175 bytes (20 words) - 14:41, 6 February 2010
• Click chemistry
  '''Click chemistry''', for which [[K. Barry Sharpless]] won the [[Nobel Prize]] in [[Chemistry Most substituted triazoles are synthesized by one of several click chemistry methods. One method uses [[palladium]] (Pd) catalysts to couple [[alkyne|al
  3 KB (437 words) - 14:16, 6 February 2010
• Triazole
  ...l compounds. Today, most substituted triazoles are produced by so-called [[click chemistry]] pioneered by [[K. Barry Sharpless]] and others (see below). Synonyms for Most substituted triazoles are synthesized by one of several click chemistry methods. One method uses [[palladium]] (Pd) catalysts to couple [[alkyne|al
  3 KB (477 words) - 13:01, 11 June 2009
• Amine gas treating
  ...y of Materials, 2007, Vol. 19, No. 15, 3581-3583</ref> (e.g., the use of [[Click chemistry]] and commodity chemicals) for the preparation of CO₂-reactive s
  9 KB (1,476 words) - 09:37, 6 March 2024
• Amine gas treating/Citable Version
  ...y of Materials, 2007, Vol. 19, No. 15, 3581-3583</ref> (e.g., the use of [[Click chemistry]] and commodity chemicals) for the preparation of CO₂-reactive s
  9 KB (1,470 words) - 09:37, 6 March 2024
• Organic reaction/Catalogs
  *[[Click chemistry]]
  19 KB (1,719 words) - 17:32, 25 March 2010