dc.contributor.author |
Kampouris, EM |
en |
dc.date.accessioned |
2014-03-01T01:37:44Z |
|
dc.date.available |
2014-03-01T01:37:44Z |
|
dc.date.issued |
1972 |
en |
dc.identifier.issn |
14727781 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/21672 |
|
dc.title |
Nitro- and amino-pyrocatechols |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1039/P19720001088 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1039/P19720001088 |
en |
heal.publicationDate |
1972 |
en |
heal.abstract |
Mononitration of pyrocatechol monobenzenesulphonate gave 4-nitropyrocatechol 2-benzenesulphonate and 3-nitropyrocatechol 1-benzenesulphonate. More vigorious conditions of nitration yielded 3,5-dinitropyrocatechol 1-benzenesulphonate. From these compounds the corresponding nitropyrocatechols and their acetates, benzene-sulphonates, and methyl ethers were prepared. Reduction of the mononitro-compounds gave the corresponding aminopyrocatechols, from which several acetyl derivatives were prepared. |
en |
heal.journalName |
Journal of the Chemical Society, Perkin Transactions 1 |
en |
dc.identifier.doi |
10.1039/P19720001088 |
en |
dc.identifier.spage |
1088 |
en |
dc.identifier.epage |
1090 |
en |