Synthesis of functionalized heterocycles via Pd-catalyzed aminocarbonylation using Mo(CO)6 as alternative CO-source and tandem cyclisation-condensation to access dihydroquinazolinones
Oschatz, Stefan Thomas
1985-
aut
text
theses
Text
Hochschulschrift
gw
2015
monographic
XA-DE
2015
eng
text/html
application/pdf
Online-Ressource Illustrationen
The aim of this work was the devewlopement of Pd-catalyzed aminocarbonylative cross coupling reactions to obtain various amide scaffolds. These syntheses were performed with the use of molybdenum hexacarbonyl as alternative CO source to avoid the application of gaseous carbon monoxide. The second part of the work focused on tandem condensation-cyclisation reactions of 2-amino-benzonitriles with aldehydes to give access to 1,2-dihydroquinazolinones. The condensation-cyclisation was furthermore performed using 2-amino-benzothioamides to allow for the synthesis of 1,2-dihydro-quinazolinthiones.
vorgelegt von Stefan Thomas Oschatz
Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2015
547.593
546.636595
547.215
540
35.69
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0195-9
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0195-9&pdf
http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2015-0195-9
Synthesis of functionalized heterocycles via Pd-catalyzed aminocarbonylation using Mo(CO)6 as alternative CO-source and tandem cyclisation-condensation to access dihydroquinazolinones
2015
Druck-Ausgabe
(DE-627)84130985X
Oschatz, Stefan Thomas, 1985 -
urn:nbn:de:gbv:28-diss2015-0195-9
935976244
rakwb
DE-627
151208
842373241
20251224T201011.0
Converted from MARCXML to MODS version 3.8 using MARC21slim2MODS3-8_XSLT1-0.xsl
(Revision 1.174 20250328)
ger