Triple

T22067610
Position Surface form Disambiguated ID Type / Status
Subject Robinson annulation reaction E545316 entity
Predicate relatedTo P37 FINISHED
Object Dieckmann condensation NE NERFINISHED

How this triple was built (3 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: Dieckmann condensation | Statement: [Robinson annulation reaction, relatedTo, Dieckmann condensation]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Dieckmann condensation
Context triple: [Robinson annulation reaction, relatedTo, Dieckmann condensation]
  • A. Barton reaction
    The Barton reaction is an organic photochemical transformation that converts nitrite esters into δ-nitroso alcohols via intramolecular hydrogen abstraction and radical rearrangement.
  • B. 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.
  • C. Heck reaction
    The Heck reaction is a palladium-catalyzed cross-coupling between alkenes and aryl or vinyl halides, widely used in organic synthesis to form carbon–carbon bonds.
  • D. Chichibabin reaction
    The Chichibabin reaction is an organic chemistry transformation that introduces an amino group into heteroaromatic compounds, especially pyridines, using sodium amide.
  • E. Diels–Kranz
    Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Dieckmann condensation
Target entity description: Dieckmann condensation is an intramolecular Claisen condensation in which a diester forms a cyclic β-keto ester under basic conditions.
  • A. Barton reaction
    The Barton reaction is an organic photochemical transformation that converts nitrite esters into δ-nitroso alcohols via intramolecular hydrogen abstraction and radical rearrangement.
  • B. 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.
  • C. Heck reaction
    The Heck reaction is a palladium-catalyzed cross-coupling between alkenes and aryl or vinyl halides, widely used in organic synthesis to form carbon–carbon bonds.
  • D. Chichibabin reaction
    The Chichibabin reaction is an organic chemistry transformation that introduces an amino group into heteroaromatic compounds, especially pyridines, using sodium amide.
  • E. Diels–Kranz
    Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
  • F. None of above. chosen

Provenance (2 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_69e11e344dfc81909b1d88a7221329c7 completed April 16, 2026, 5:36 p.m.
NER Named-entity recognition batch_69f12884937c819095d3af69123fa2cb completed April 28, 2026, 9:37 p.m.
Created at: April 16, 2026, 8:27 p.m.