PMC:7571312 / 11799-12006
Annnotations
LitCovid-PD-CLO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T64722 | 0-1 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | A |
| T21026 | 205-207 | http://purl.obolibrary.org/obo/CLO_0001000 | denotes | 35 |
LitCovid-PD-CHEBI
| Id | Subject | Object | Predicate | Lexical cue | chebi_id |
|---|---|---|---|---|---|
| T165 | 82-86 | Chemical | denotes | acid | http://purl.obolibrary.org/obo/CHEBI_37527 |
| T166 | 110-123 | Chemical | denotes | Weinreb amide | http://purl.obolibrary.org/obo/CHEBI_59741 |
| T167 | 118-123 | Chemical | denotes | amide | http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988 |
| T169 | 179-185 | Chemical | denotes | benzyl | http://purl.obolibrary.org/obo/CHEBI_22744 |
| T170 | 199-204 | Chemical | denotes | ether | http://purl.obolibrary.org/obo/CHEBI_25698 |
LitCovid-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T60 | 0-207 | Sentence | denotes | A direct approach to oxymethylketone intermediate 9 was achieved by conversion of acid 6 to the corresponding Weinreb amide followed by treatment with the Grignard generated from benzyl chloromethyl ether.35 |
LitCovid-PubTator
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 293 | 21-36 | Chemical | denotes | oxymethylketone |
| 294 | 110-123 | Chemical | denotes | Weinreb amide |
| 295 | 179-204 | Chemical | denotes | benzyl chloromethyl ether |