Westphalen–Lettré Rearrangement
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Westphalen–Lettré Rearrangement
The Westphalen–Lettré rearrangement is a classic organic reaction in organic chemistry describing a rearrangement reaction of cholestane, cholestane-3β,5α,6β-triol diacetate with acetic anhydride and sulfuric acid. In this reaction one equivalent of water is lost, a double bond is formed at C10–C11 and importantly the methyl group at the C10 position migrates to the C5 position. The reaction is Order of reaction, first-order in steroid in the presence of an excess of sulfuric acid''Acid catalysed reactions of 5α-hydroxy-steroids—III : The westphalen rearrangement''Tetrahedron, Volume 21, Issue 6, 1965, Pages 1567–1580 J. W. Blunt, A. Fischer, M. P. Hartshorn, F. W. Jones, Kirk D. N. and S. W. Yoong () and the first reaction step in the reaction mechanism is likely the formation of a sulfate ester followed by that of a carbocation at C5 after which the actual re-arrangement takes place. References

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Organic Reaction
Organic reactions are chemical reactions involving organic compounds. The basic organic chemistry reaction types are addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions, Mechanistic Organic Photochemistry, photochemical reactions and organic redox reaction, redox reactions. In organic synthesis, organic reactions are used in the construction of new organic molecules. The production of many man-made chemicals such as drugs, plastics, food additives, fabrics depend on organic reactions. The oldest organic reactions are combustion of organic fuels and saponification of fats to make soap. Modern organic chemistry starts with the Wöhler synthesis in 1828. In the history of the Nobel Prize in Chemistry awards have been given for the invention of specific organic reactions such as the Grignard reaction in 1912, the Diels-Alder reaction in 1950, the Wittig reaction in 1979 and olefin metathesis in 2005. Classifications Organic c ...
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