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.