Triple

T21337723
Position Surface form Disambiguated ID Type / Status
Subject Charles J. Pedersen E526093 entity
Predicate notableWork P4 FINISHED
Object Synthesis of crown ethers 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: Synthesis of crown ethers | Statement: [Charles J. Pedersen, notableWork, Synthesis of crown ethers]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Synthesis of crown ethers
Context triple: [Charles J. Pedersen, notableWork, Synthesis of crown ethers]
  • A. Corey–Nicolaou macrolactonization
    Corey–Nicolaou macrolactonization is a widely used organic synthesis reaction that forms large-ring lactones from hydroxy acids via an activated ester intermediate.
  • B. Mitsunobu macrolactonization
    Mitsunobu macrolactonization is a variant of the Mitsunobu reaction used in organic synthesis to form large-ring lactones by intramolecular esterification under mild, dehydrative conditions.
  • C. The Logic of Chemical Synthesis
    The Logic of Chemical Synthesis is a seminal book by chemist Elias J. Corey that systematically presents the principles and strategies of retrosynthetic analysis for designing complex organic molecule syntheses.
  • D. Yamaguchi macrolactonization
    Yamaguchi macrolactonization is a widely used organic synthesis method for forming large-ring lactones via intramolecular esterification activated by a mixed anhydride, particularly valuable in complex natural product synthesis.
  • E. Enantioselective Chemical Synthesis
    Enantioselective Chemical Synthesis is a foundational work in organic chemistry that systematically presents strategies and methods for constructing chiral molecules with high stereocontrol.
  • 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: Synthesis of crown ethers
Target entity description: "Synthesis of crown ethers" is the landmark work in which chemist Charles J. Pedersen first reported the creation of crown ether compounds, foundational molecules in host–guest and supramolecular chemistry.
  • A. Corey–Nicolaou macrolactonization
    Corey–Nicolaou macrolactonization is a widely used organic synthesis reaction that forms large-ring lactones from hydroxy acids via an activated ester intermediate.
  • B. Mitsunobu macrolactonization
    Mitsunobu macrolactonization is a variant of the Mitsunobu reaction used in organic synthesis to form large-ring lactones by intramolecular esterification under mild, dehydrative conditions.
  • C. The Logic of Chemical Synthesis
    The Logic of Chemical Synthesis is a seminal book by chemist Elias J. Corey that systematically presents the principles and strategies of retrosynthetic analysis for designing complex organic molecule syntheses.
  • D. Yamaguchi macrolactonization
    Yamaguchi macrolactonization is a widely used organic synthesis method for forming large-ring lactones via intramolecular esterification activated by a mixed anhydride, particularly valuable in complex natural product synthesis.
  • E. Enantioselective Chemical Synthesis
    Enantioselective Chemical Synthesis is a foundational work in organic chemistry that systematically presents strategies and methods for constructing chiral molecules with high stereocontrol.
  • 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_69e0b51c33048190ab27cede74ef798c completed April 16, 2026, 10:08 a.m.
NER Named-entity recognition batch_69e898da015081909e83fb62cf166b9a completed April 22, 2026, 9:46 a.m.
Created at: April 16, 2026, 4:43 p.m.