organic reaction
C22930
concept
An organic reaction is a chemical transformation involving organic compounds, where bonds between carbon and other atoms are broken and formed to yield new molecular structures.
All labels observed (15)
| Label | Occurrences |
|---|---|
| organic reaction canonical | 18 |
| cross-coupling reaction | 2 |
| cycloaddition reaction | 2 |
| Norrish reaction subtype | 1 |
| aldol reaction | 1 |
| allylic substitution reaction | 1 |
| annulation reaction | 1 |
| asymmetric catalysis method | 1 |
| chiral auxiliary methodology | 1 |
| enantioselective synthesis method | 1 |
| hydroboration reaction | 1 |
| macrolactonization reaction | 1 |
| olefination reaction | 1 |
| organoborane chemistry method | 1 |
| pericyclic reaction | 1 |
Description generation (CDg)
The one-sentence description above was generated by prompting gpt-5.1 with the class name and this instruction.
Instruction
generate a one-sentence description for a given conceptual class. # Response Format Return only the sentence: "Description: [one-sentence description of the conceptional class]"
Input
Class: organic reaction
Generated description
An organic reaction is a chemical transformation involving organic compounds, where bonds between carbon and other atoms are broken and formed to yield new molecular structures.
Instances (24)
| Instance | Via concept surface |
|---|---|
| Shi epoxidation | — |
| Fischer esterification | — |
| Sharpless epoxidation | enantioselective synthesis method |
| Suzuki coupling | cross-coupling reaction |
| Buchwald–Hartwig amination | cross-coupling reaction |
| Barton reaction | — |
| Barton–McCombie deoxygenation | — |
| Eschenmoser–Claisen rearrangement | — |
| Eschenmoser–Tanabe fragmentation | — |
| Eschenmoser sulfide contraction | — |
| Trost asymmetric allylic alkylation | asymmetric catalysis method |
| Corey–Bakshi–Shibata reduction | — |
| Corey–Winter olefin synthesis | — |
| Corey–Nicolaou macrolactonization | — |
| Robinson annulation reaction | — |
|
Norrish reaction
surface form:
Norrish type I reaction
|
Norrish reaction subtype |
| Brown hydroboration | — |
| Evans auxiliary-based asymmetric synthesis | chiral auxiliary methodology |
| Evans aldol reaction | — |
| Stork enamine reaction | — |
| Stork–Danheiser rearrangement | — |
| Diels–Alder reaction | pericyclic reaction |
|
Diels
surface form:
Diels–Alder reaction
|
cycloaddition reaction |
| Overman rearrangement | — |