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In organic chemistry, the acetoxy group (abbr. AcO– or –OAc; IUPAC name: acetyloxy), is a functional group with the formula .mw-parser-output .template-chem2-su{display:inline-block;font-size:80%;line-height:1;vertical-align:-0.35em}.mw-parser-output .template-chem2-su>span{display:block;text-align:left}.mw-parser-output…
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group acetoxy alcohol acetyl base presence name ch3 functionality also like acid form protection deprotection acetylation ester aqueous formula structure
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| pyridine with a bit of DMAP added.An alcohol is not a particularly strong nucleophile and | instance of | although this is not advisable due to higher costs and difficulties.Acetic anhydride in the presence of base with a catalyst | 0.80 | text |
| when present | instance of | although this is not advisable due to higher costs and difficulties.Acetic anhydride in the presence of base with a catalyst | 0.80 | text |
| more powerful nucleophiles like amines will react with the above-mentioned reagents in preference to the alcohol.Alcohol deprotectionFor deprotection | instance of | although this is not advisable due to higher costs and difficulties.Acetic anhydride in the presence of base with a catalyst | 0.80 | text |
| more powerful nucleophiles like amines will react with the above-mentioned reagents in preference to the alcohol | instance of | although this is not advisable due to higher costs and difficulties.Acetic anhydride in the presence of base with a catalyst | 0.80 | text |
| sodium methoxide in methanol | instance of | may have to be heatedAnhydrous base | 0.80 | text |
| Acetoxy group | related to Functionality | An | 0.60 | section |
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