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.

Stille reaction · Vinony

EntityQ899861· pop 20· linked from 270 articles

Stille reaction

Sign in to save

chemical reaction used in organic synthesis

Connections

cross-coupling reaction

cis–trans isomerism

chemical polarity

Angewandte Chemie

Sonogashira coupling

transmetalation

trifluoromethanesulfonate

directing group

Categories

Carbon-carbon bond forming reactions Citation overkill Name reactions Palladium

Sources

wikipedia.externallinksexternallink

Similar entities

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

Stollé synthesis

Entitydist 0.40

Vilsmeier–Haack reaction

Entitydist 0.54

tert-butyl hydroperoxide

Entitydist 0.56

Nenitzescu indole synthesis

Entitydist 0.58

tert-butyl nitrite

Entitydist 0.58

Bartoli indole synthesis

Entitydist 0.59

hydrogen peroxide

Entitydist 0.59

hydrogen cyanide

Entitydist 0.61

Entitydist 0.61

Pummerer rearrangement

Entitydist 0.61

N-formyl-L-kynurenine

Entitydist 0.61

Entitydist 0.62

What links here270 pages

cross-coupling reaction

Kumada coupling

1,2-Wittig rearrangement

Creighton process

Bischler–Napieralski reaction

Corey–House synthesis

Bingel reaction

copper chromite

Allylic rearrangement

enyne metathesis

Bucherer reaction

Biginelli reaction

Michael reaction

Algar–Flynn–Oyamada reaction

potassium permanganate

Bodroux–Chichibabin aldehyde synthesis

transmetalation

Barton decarboxylation

Hiyama coupling

Combes quinoline synthesis

Barton–Kellogg reaction