Skip to content

Sections

Maps Timeline Graph Cosmos Life Culture Innovation People Climate Trends Art

© 2026 Vinony · Knowledge from Wikipedia, Wikidata, and 27 public APIs.

Kauffmann olefination · Vinony

EntityQ906093· pop 6· linked from 255 articles

Kauffmann olefination

Sign in to save

type of chemical reaction

Connections

digital object identifier

Friedel–Crafts reaction

hydration reaction

Diels–Alder reaction

Categories

Carbon-carbon bond forming reactions Name reactions Olefination reactions

Sources

wikipedia.externallinksexternallink

Similar entities

Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).

Entitydist 0.45

Entitydist 0.51

Saegusa–Ito oxidation

Entitydist 0.52

ibandronic acid

Entitydist 0.52

Dechlorane plus

Entitydist 0.53

Varrentrapp reaction

Entitydist 0.53

Entitydist 0.53

1-chloro-2-propanol

Entitydist 0.53

Entitydist 0.53

propanoyl chloride

Entitydist 0.53

cyanogen iodide

Entitydist 0.53

Entitydist 0.54

What links here255 pages

Borsche–Drechsel cyclization

1,2-Wittig rearrangement

Bischler–Napieralski reaction

Bamberger triazine synthesis

copper chromite

Creighton process

Corey–House synthesis

Bingel reaction

enyne metathesis

Allylic rearrangement

Hofmann elimination

Bucherer reaction

Algar–Flynn–Oyamada reaction

potassium permanganate

Biginelli reaction

Bodroux–Chichibabin aldehyde synthesis

Barton decarboxylation

Combes quinoline synthesis

cross-coupling reaction

Barton–Kellogg reaction

Cadogan-Sundberg indole synthesis

Auwers synthesis