Triple

T13307980
Position Surface form Disambiguated ID Type / Status
Subject K. Barry Sharpless E316985 entity
Predicate knownFor P22 FINISHED
Object Sharpless epoxidation E316986 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: Sharpless epoxidation | Statement: [K. Barry Sharpless, knownFor, Sharpless epoxidation]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Sharpless epoxidation
Context triple: [K. Barry Sharpless, knownFor, Sharpless epoxidation]
  • A. Sharpless epoxidation chosen
    Sharpless epoxidation is a landmark asymmetric oxidation reaction in organic chemistry that enables the enantioselective conversion of allylic alcohols to epoxides using chiral catalysts.
  • B. Sharpless asymmetric dihydroxylation
    Sharpless asymmetric dihydroxylation is a landmark chemical reaction that uses chiral catalysts to add two hydroxyl groups across an alkene with high enantioselectivity, revolutionizing asymmetric synthesis in organic chemistry.
  • C. Corey–Kim oxidation
    Corey–Kim oxidation is an organic chemistry reaction that converts primary and secondary alcohols into aldehydes and ketones using N-chlorosuccinimide and dimethyl sulfide under mild conditions.
  • D. 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.
  • E. Corey–Winter olefin synthesis
    Corey–Winter olefin synthesis is an organic reaction that converts 1,2-diols into alkenes via cyclic thiocarbonate intermediates, widely used for stereospecific formation of double bonds.
  • 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_69d806b40ab4819094adf6c374f4811a completed April 9, 2026, 8:06 p.m.
NER Named-entity recognition batch_69d990a8be108190bad0021f95ce3a93 completed April 11, 2026, 12:07 a.m.
NED1 Entity disambiguation (via context triple) batch_69f716e58cc48190afb46e8394227ab5 completed May 3, 2026, 9:35 a.m.
Created at: April 9, 2026, 9:29 p.m.