Triple
T13308182
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | click chemistry |
E316989
|
entity |
| Predicate | coreReactionType |
P82471
|
FINISHED |
| Object | CuAAC |
E316989
|
NE FINISHED |
How this triple was built (2 steps)
Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.
NER
Named-entity recognition
gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: CuAAC | Statement: [click chemistry, coreReactionType, CuAAC]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: CuAAC Context triple: [click chemistry, coreReactionType, CuAAC]
-
A.
Buchwald–Hartwig amination
The Buchwald–Hartwig amination is a palladium-catalyzed cross-coupling reaction that forms carbon–nitrogen bonds by coupling aryl (or vinyl) halides with amines, widely used in the synthesis of pharmaceuticals and fine chemicals.
-
B.
click chemistry
chosen
Click chemistry is a modular, high-yielding approach to chemical synthesis that uses simple, reliable reactions to rapidly assemble complex molecules, widely applied in drug discovery, materials science, and chemical biology.
-
C.
Suzuki coupling
Suzuki coupling is a widely used palladium-catalyzed cross-coupling reaction that forms carbon–carbon bonds between organoboron compounds and organic halides, fundamental in organic synthesis and pharmaceutical chemistry.
-
D.
Diels–Alder reaction
The Diels–Alder reaction is a fundamental organic chemistry cycloaddition that forms six-membered rings by combining a conjugated diene with a dienophile in a single, stereospecific step.
-
E.
Eschenmoser sulfide contraction
Eschenmoser sulfide contraction is an organic rearrangement reaction that converts certain sulfur-containing intermediates into carbonyl compounds, widely used in complex molecule and natural product synthesis.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (3 batches)
The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.
| Step | Stage | Batch ID | Status | When |
|---|---|---|---|---|
| creating | Elicitation | batch_69d806b40ab4819094adf6c374f4811a |
completed | April 9, 2026, 8:06 p.m. |
| NER | Named-entity recognition | batch_69dadcd4cb008190af99c4856e76ac08 |
completed | April 11, 2026, 11:44 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69f716e58cc48190afb46e8394227ab5 |
completed | May 3, 2026, 9:35 a.m. |
Created at: April 9, 2026, 9:29 p.m.