Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(?-ketoacyl)anthranilic acids.

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28610%2F13%3A43869978" target="_blank" >RIV/70883521:28610/13:43869978 - isvavai.cz</a>
Alternative codes found
RIV/70883521:28110/13:43869978
Result on the web
<a href="http://ac.els-cdn.com/S0040402013016530/1-s2.0-S0040402013016530-main.pdf?_tid=931e8910-6bf0-11e3-b7b5-00000aacb35e&acdnat=1387816855_d46c9cf9df5b87f769c4c57050cb8620" target="_blank" >http://ac.els-cdn.com/S0040402013016530/1-s2.0-S0040402013016530-main.pdf?_tid=931e8910-6bf0-11e3-b7b5-00000aacb35e&acdnat=1387816855_d46c9cf9df5b87f769c4c57050cb8620</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.tet.2013.10.092" target="_blank" >10.1016/j.tet.2013.10.092</a>

Result language
angličtina
Original language name
Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(?-ketoacyl)anthranilic acids.
Original language description
N-(?-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is described as well as the utilisation of N-(?-ketoacyl)anthranilic acids in the preparation of anthranilic acid hydrochlorides.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Similar results(10)