| dc.contributor.author |
Szymor-Pietrzak, Damian |
|
| dc.contributor.author |
Khan, Muhammad N. |
|
| dc.contributor.author |
Pag�s, Ana�s |
|
| dc.contributor.author |
Kumar, Ajay |
|
| dc.contributor.author |
Depner, Noah |
|
| dc.contributor.author |
Clive, Derrick L. J |
|
| dc.coverage.spatial |
United States of America |
|
| dc.date.accessioned |
2020-12-09T14:01:04Z |
|
| dc.date.available |
2020-12-09T14:01:04Z |
|
| dc.date.issued |
2020-12 |
|
| dc.identifier.citation |
Szymor-Pietrzak, Damian; Khan, Muhammad N.; Pagès, Anaïs; Kumar, Ajay; Depner, Noah and Clive, Derrick L. J., “Formation of 3-Aminophenols from Cyclohexane-1,3-diones”, Journal of Organic Chemistry, DOI: 10.1021/acs.joc.0c02284, Dec. 2020. |
en_US |
| dc.identifier.issn |
0022-3263 |
|
| dc.identifier.issn |
1520-6904 |
|
| dc.identifier.uri |
https://doi.org/10.1021/acs.joc.0c02284 |
|
| dc.identifier.uri |
https://repository.iitgn.ac.in/handle/123456789/6120 |
|
| dc.description.abstract |
meta-Aminophenols are formed by the action of DBU on 3-amino-2-chlorocyclohex-2-en-1-ones at room temperature in MeCN. The chloro compounds are generated by treating 3-aminocyclohex-2-en-1-ones with the easily prepared halogenating agent BnNMe3·ICl2 in MeOH-CH2Cl2. The amino group must carry two substituents, either two aryl, one aryl and one alkyl, or two alkyl groups; 3-aminocyclohex-2-en-1-ones of this type are readily made from cyclohex-2-en-1-one and a primary or secondary amine. |
|
| dc.description.statementofresponsibility |
by Damian Szymor-Pietrzak, Muhammad N. Khan, Ana�s Pag�s, Ajay Kumar, Noah Depner, and Derrick L. J. Clive |
|
| dc.language.iso |
en_US |
en_US |
| dc.publisher |
American Chemical Society |
en_US |
| dc.title |
Formation of 3-Aminophenols from Cyclohexane-1,3-diones |
en_US |
| dc.type |
Article |
en_US |
| dc.relation.journal |
Journal of Organic Chemistry |
|