Category
page 1Rearrangement reactions
rearrangement reaction
organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule
Hofmann rearrangement
type of chemical reaction
pericyclic reaction
organic chemical reaction wherein the transition state of the molecule has a cyclic geometry, the reaction progresses in concert, and the bond orbitals involved overlap in a continuous cycle at the transition state
Beckmann rearrangement
chemical rearrangement
Curtius rearrangement
chemical reaction
Bamberger rearrangement
name reaction
Claisen rearrangement
chemical reaction
Wolff rearrangement
Chemical reaction
Neber rearrangement
rearrangement of O-sulfonates of ketoximes under the action of strong bases into azirines and further into α-aminoketones
pinacol rearrangement
rearrangement of a 1,2-diol compound to carbonyl compound
electrocyclic reaction
Fries rearrangement
rearrangement reaction of a phenolic ester to a keto-substituted phenol
Cope rearrangement
Organic chemical reaction
Nazarov cyclization reaction
Chemical reaction used in organic chemistry
Amadori rearrangement
Organic reaction: isomerization or rearrangement reaction of the N-glycoside of an aldose or the glycosylamine to the corresponding 1-amino-1-deoxy-ketose
sigmatropic reaction
chemical reaction
Favorskii rearrangement
chemical reaction
Favorskii reaction
Chemical reaction
ene reaction
chemical reaction
Wagner–Meerwein rearrangement
organic reaction
Arndt–Eistert reaction
series of chemical reactions
McLafferty rearrangement
Chemical reaction
Brook rearrangement
rearrangement in organic chemistry
Hayashi rearrangement
chemical reaction
Pummerer rearrangement
reaction in organic chemistry
Schmidt reaction
Azide reacts with a carbonyl group to give amine/amide(ketone)
Fischer–Hepp rearrangement
organic reaction applied to aromatic nitroso and nitrosamine compounds
Dimroth rearrangement
Chemical reaction
Benzilic acid rearrangement
rearrangement reaction
Meyer–Schuster rearrangement
Chemical reaction
Corey–Fuchs reaction
series of chemical reactions designed to transform an aldehyde into an alkyne
Smiles rearrangement
chemical reaction
Lossen rearrangement
conversion of a hydroxamic acid to an isocyanate
Chan rearrangement
Chemical reaction
Overman rearrangement
Criegee rearrangement
rearrangement reaction
Demjanov rearrangement
chemical reaction
1,2-Wittig rearrangement
categorization of chemical reactions
Allylic rearrangement
type of organic chemical reaction
Carroll rearrangement
chemical reaction
Baker–Venkataraman rearrangement
chemical reaction discovered by and named after W. Baker and K. Venkataraman
Willgerodt rearrangement
Chemical reaction
Lobry de Bruyn–Van Ekenstein transformation
rearrangement reaction
Bergman cyclization
rearrangement reaction taking place when an enediyne is heated in presence of a suitable hydrogen donor
Ireland–Claisen rearrangement
chemical reaction
Hofmann–Martius rearrangement
chemical reaction
1,2-rearrangement
A 1,2-rearrangement or 1,2-migration or 1,2-shift or Whitmore 1,2-shift is an organic reaction where a substituent moves from one atom to another atom in a chemical compound. In a 1,2 shift the movement involves two adjacent atoms but moves over larger distances are possible. In the example below the substituent R moves from carbon atom C2 to C3.
Mumm rearrangement
Fritsch–Buttenberg–Wiechell rearrangement
Chemical reaction series
Gabriel–Colman rearrangement
chemical reaction
Bergmann degradation
chemical reaction
Sommelet–Hauser rearrangement
New alkyl group in the aromatic ortho position
Buchner ring expansion
chemical reaction
Wallach rearrangement
organic reaction converting an azoxy compound to an azo compound
Dowd–Beckwith ring-expansion reaction
organic reaction
Seyferth–Gilbert homologation
chemical reaction
Westphalen–Lettré rearrangement
McFadyen–Stevens reaction
chemical reaction
vinylcyclopropane rearrangement
chemical reaction
Weerman degradation
reaction in organic chemistry