Curtius rearrangement: Difference between revisions
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The '''Curtius rearrangement''' was first reported by Theodor Curtius in 1890. This rearrangement which is sometimes also called the Curtius reaction or Curtius degradation proceeds via a highly versatile isocyanate intermediate which can be easily trapped by a variety of nucleophiles, including water, alcohols, and amines via a concerted mechanism which proceeds with retention of configuration. Therefore, this Curtius rearrangement is one of the most widely used organic reactions, with numerous recent examples in the literature. | {{subpages}} | ||
The '''Curtius rearrangement''' was first reported by Theodor Curtius in 1890. This rearrangement which is sometimes also called the Curtius reaction or Curtius degradation proceeds via a highly versatile isocyanate intermediate which can be easily trapped by a variety of nucleophiles, including water, alcohols, and amines via a concerted mechanism which proceeds with retention of configuration. Therefore, this Curtius rearrangement is one of the most widely used organic reactions, with numerous recent examples in the literature. | |||
Revision as of 18:12, 20 December 2007
The Curtius rearrangement was first reported by Theodor Curtius in 1890. This rearrangement which is sometimes also called the Curtius reaction or Curtius degradation proceeds via a highly versatile isocyanate intermediate which can be easily trapped by a variety of nucleophiles, including water, alcohols, and amines via a concerted mechanism which proceeds with retention of configuration. Therefore, this Curtius rearrangement is one of the most widely used organic reactions, with numerous recent examples in the literature.