| 31. | Finally, the acyl azide reacts in the normal manner to give the urethane.
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| 32. | If you plan on actually making sodium azide, please be careful with it.
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| 33. | The free hydroxyl of this was subsequently substituted by an azide to give 32.
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| 34. | It was first obtained by Theodor Curtius in 1890, along with other azides.
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| 35. | Azides are cleanly reduced to amines in preference to sterically hindered aliphatic nitro groups:
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| 36. | The monomers used in this polymerization are oligopeptides with terminal azide and terminal alkyne groups
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| 37. | This 2-hydroxy structure is then reacted with azide and a nucleophilic base.
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| 38. | Sodium azide is a hazardous substance, highly explosive and tricky to handle in manufacturing.
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| 39. | Sodium azide is a notoriously dangerous chemical.
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| 40. | Sodium azide increases cyclic GMP levels in brain and liver by activation of guanylate cyclase.
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