Triple

T13176858
Position Surface form Disambiguated ID Type / Status
Subject K. C. Nicolaou E313119 entity
Predicate notableWork P4 FINISHED
Object Classics in Total Synthesis III E1027562 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: Classics in Total Synthesis III | Statement: [K. C. Nicolaou, notableWork, Classics in Total Synthesis III]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Classics in Total Synthesis III
Context triple: [K. C. Nicolaou, notableWork, Classics in Total Synthesis III]
  • A. Classics in Total Synthesis chosen
    Classics in Total Synthesis is a highly influential chemistry book that showcases landmark strategies and case studies in the total synthesis of complex natural products.
  • B. 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.
  • C. 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.
  • D. 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.
  • 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_69d806ac3ee081909b2fd27d060aa974 completed April 9, 2026, 8:06 p.m.
NER Named-entity recognition batch_69d98c322fdc8190b05f2287eba9dda6 completed April 10, 2026, 11:48 p.m.
NED1 Entity disambiguation (via context triple) batch_69f70a2a3f2881909af3e146ee24062d completed May 3, 2026, 8:41 a.m.
Created at: April 9, 2026, 9:14 p.m.