Triple

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).

Phrase: Corey–Chaykovsky epoxidation | Statement: [Corey–Chaykovsky reagent, relatedReaction, Corey–Chaykovsky epoxidation]

Target entity: Corey–Chaykovsky epoxidation
Context triple: [Corey–Chaykovsky reagent, relatedReaction, Corey–Chaykovsky epoxidation]

• A. Shi epoxidation
  Shi epoxidation is an asymmetric organocatalytic reaction that converts alkenes to chiral epoxides using a fructose-derived ketone catalyst and an oxidant such as oxone.
• B. Sharpless epoxidation
  Sharpless epoxidation is a landmark asymmetric oxidation reaction in organic chemistry that enables the enantioselective conversion of allylic alcohols to epoxides using chiral catalysts.
• 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. 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.
• E. 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.
• F. None of above. chosen
• G. Unsure - the case is ambiguous/there is not enough information to decide.

Target entity: Corey–Chaykovsky epoxidation
Target entity description: The Corey–Chaykovsky epoxidation is an organic reaction that converts carbonyl compounds into epoxides using sulfur ylides derived from sulfonium or sulfoxonium salts.

• A. Shi epoxidation
  Shi epoxidation is an asymmetric organocatalytic reaction that converts alkenes to chiral epoxides using a fructose-derived ketone catalyst and an oxidant such as oxone.
• B. Sharpless epoxidation
  Sharpless epoxidation is a landmark asymmetric oxidation reaction in organic chemistry that enables the enantioselective conversion of allylic alcohols to epoxides using chiral catalysts.
• 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. 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.
• E. 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.
• F. None of above. chosen