Triple
T4418987
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Richard R. Schrock |
E95049
|
entity |
| Predicate | notableConcept |
P201
|
FINISHED |
| Object |
Schrock carbene
A Schrock carbene is a type of organometallic complex featuring an early transition metal bonded to a strongly nucleophilic alkylidene ligand, central to many olefin metathesis catalysts.
|
E438047
|
NE FINISHED |
How this triple was built (4 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: Schrock carbene | Statement: [Richard R. Schrock, notableConcept, Schrock carbene]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Schrock carbene Context triple: [Richard R. Schrock, notableConcept, Schrock carbene]
-
A.
Eschenmoser
Eschenmoser is a Swiss surname most notably associated with Albert Eschenmoser, a prominent organic chemist known for his pioneering work in the synthesis of complex natural products and studies on the origin of life.
-
B.
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.
-
C.
Eschenmoser–Claisen rearrangement
The Eschenmoser–Claisen rearrangement is a variant of the Claisen rearrangement in organic chemistry that converts allylic alcohols and amides into γ,δ-unsaturated carbonyl compounds via a [3,3]-sigmatropic rearrangement.
-
D.
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.
-
E.
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.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg
Description generation
gpt-5.1
Instruction
Generate a one-sentence description of the target entity. You are given a context triple in the form (subject, predicate, object), where the object is the target entity. # Instructions Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. Avoid repeating the information from the triple, unless really essential. # Response Format Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: Schrock carbene Triple: [Richard R. Schrock, notableConcept, Schrock carbene]
Generated description
A Schrock carbene is a type of organometallic complex featuring an early transition metal bonded to a strongly nucleophilic alkylidene ligand, central to many olefin metathesis catalysts.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Schrock carbene Target entity description: A Schrock carbene is a type of organometallic complex featuring an early transition metal bonded to a strongly nucleophilic alkylidene ligand, central to many olefin metathesis catalysts.
-
A.
Eschenmoser
Eschenmoser is a Swiss surname most notably associated with Albert Eschenmoser, a prominent organic chemist known for his pioneering work in the synthesis of complex natural products and studies on the origin of life.
-
B.
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.
-
C.
Eschenmoser–Claisen rearrangement
The Eschenmoser–Claisen rearrangement is a variant of the Claisen rearrangement in organic chemistry that converts allylic alcohols and amides into γ,δ-unsaturated carbonyl compounds via a [3,3]-sigmatropic rearrangement.
-
D.
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.
-
E.
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.
- F. None of above. chosen
Provenance (5 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_69b3453a36908190b95a79a297ca083c |
completed | March 12, 2026, 10:59 p.m. |
| NER | Named-entity recognition | batch_69b3551e7c6c819090fa5dfb5ac58e4c |
completed | March 13, 2026, 12:06 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69b5f623c958819087630c16b6ac8cb8 |
completed | March 14, 2026, 11:58 p.m. |
| NEDg | Description generation | batch_69b5f9f26ef88190842e01d952e52125 |
completed | March 15, 2026, 12:14 a.m. |
| NED2 | Entity disambiguation (via description) | batch_69b5faa6bfe881908a76c6c54f89feda |
completed | March 15, 2026, 12:17 a.m. |
Created at: March 12, 2026, 11:29 p.m.