The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted...

The Stieglitz rearrangement is a rearrangement reaction in organic chemistry which is named after the American chemist Julius Stieglitz (1867–1937) and...

of lactams. Lactams form by the acid-catalyzed rearrangement of oximes in the Beckmann rearrangement. Lactams form from cyclic ketones and hydrazoic...

1,3-rearrangements take place over 3 carbon atoms. Examples: the Fries rearrangement a 1,3-alkyl shift of verbenone to chrysanthenone Beckmann rearrangement...

a 1,2-rearrangement: 1,2-Wittig rearrangement Alpha-ketol rearrangement Beckmann rearrangement Benzilic acid rearrangement Brook rearrangement Criegee...

obtained by Beckmann rearrangement can be transformed into a carboxylic acid by means of hydrolysis (base or acid catalyzed). Beckmann rearrangement is used...

The Neber rearrangement is an organic reaction in which a ketoxime is converted into an alpha-aminoketone via a rearrangement reaction. The oxime is first...

Beckmann rearrangement. Ernst Otto Beckmann was born in Solingen, Germany on July 4, 1853, to a family headed by Johannes Friedrich Wilhelm Beckmann,...

mono-amide, followed by a Hofmann rearrangement Beckmann rearrangement Curtius rearrangement Iodoform reaction Lossen rearrangement Schmidt reaction Weerman degradation...

doi:10.1002/jlac.18751750305. Curtius rearrangement Hofmann rearrangement Schmidt reaction Beckmann rearrangement Gabapentin Wang, Zerong (2010). Comprehensive...