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
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Amadori rearrangement
Summary
Amadori rearrangement is a type of chemical reaction[1]. It draws 55 Wikipedia views per month (type_of_chemical_reaction category, ranking #34 of 230).[2]
Key Facts
- Amadori rearrangement's instance of is recorded as type of chemical reaction[3].
- Mario Amadori is named after Amadori rearrangement[4].
- Amadori rearrangement's Commons category is recorded as Amadori rearrangement[5].
- Amadori rearrangement's Freebase ID is recorded as /m/0268cg3[6].
- Amadori rearrangement's Gran Enciclopèdia Catalana ID is recorded as 0003299[7].
- Amadori rearrangement's Merck Index reaction ID is recorded as 8[8].
- Amadori rearrangement's Microsoft Academic ID is recorded as 118094880[9].
- Amadori rearrangement's Lex ID is recorded as Amadori-omlejring[10].
- Amadori rearrangement's OpenAlex ID is recorded as C118094880[11].
- Amadori rearrangement's ScienceDirect topic ID is recorded as agricultural-and-biological-sciences/amadori-rearrangement[12].
- Amadori rearrangement's Gran Enciclopèdia Catalana ID is recorded as transposicio-damadori[13].
Why It Matters
Amadori rearrangement draws 55 Wikipedia views per month (type_of_chemical_reaction category, ranking #34 of 230).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[14] It is known by 4 alternative names across languages and contexts.[15]