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• Tetrazole
  ...]], reacting a [[cyanide]] with an [[azide]], as depicted below. The base tetrazole compound (R₁ = R₂ = H) is commonly used as a [[base ( {{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/Definition
  130 bytes (20 words) - 14:35, 6 February 2010
• Tetrazole/External Links
  143 bytes (21 words) - 14:39, 6 February 2010
• Tetrazole/Related Articles
  175 bytes (20 words) - 14:41, 6 February 2010

Page text matches

• Tetrazole
  ...]], reacting a [[cyanide]] with an [[azide]], as depicted below. The base tetrazole compound (R₁ = R₂ = H) is commonly used as a [[base ( {{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
• Heterocycle/Related Articles
  {{r|tetrazole}}
  725 bytes (102 words) - 13:06, 17 May 2008
• Click chemistry
  ...azide with a cyano compound (R-CN) produces a 2,5-disubstituted 1,2,3,4-[[tetrazole]]. {{Image|Tetrazole Click chemistry.png|right|350px|Tetrazole formed by cyclization of a cyanide and an azide.}}
  3 KB (437 words) - 14:16, 6 February 2010
• DNA synthesis (chemical)
  ...of the DNA is then promoted by the addition of an "activator", typically [[tetrazole]], a weak acid, and a phosphoramidite (<b>Scheme 2</b>). The weak acid act {{Image|Phosphoramidite elongation reaction.png|right|300px|<b>Scheme 2</b>. Tetrazole activated nucleophilic attack of base-1 5'-oxygen to the phosphorus atom of
  12 KB (1,804 words) - 09:16, 6 March 2024