Synthesis of functionalized quinolines, flavones, coumarins, naphthoates and phthalates by site-selective Suzuki-Miyaura cross-coupling reactions
Eleya, Nadi Fakhry
1978-
aut
text
theses
Text
Hochschulschrift
gw
2012
monographic
XA-DE
2012
eng
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application/pdf
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This thesis includes regioselective palladium(0)-catalyzed Suzuki cross-coupling reactions of quinolines, flavones, coumarins, naphthaoates and phthalates. Suzuki cross-coupling reaction of 5,7-dibromo-8-(trifluoromethanesulfonyloxy)quinoline afforded arylated quinolines.The Suzuki reaction of the bis(triflates)of 5,7-dihydroxyflavone,4-methyl-5,7-dihydroxycoumarin,4-methyl-5,8-dihydroxycoumarin, ethyl 3,5-dihydroxy-2-naphthaoate and methyl 3,7-dihydroxy-2-naphthoate gave the corresponding arylated derivatives. The reaction of tetrabromophthalate with boronic acids gave tetraarylphthalates.
vorgelegt von Nadi Fakhry Eleya
Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2012
35.69
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2012-0067-9
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2012-0067-9&pdf
http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2012-0067-9
Synthesis of functionalized quinolines, flavones, coumarins, naphthoates and phthalates by site-selective Suzuki-Miyaura cross-coupling reactions
2012
Druck-Ausgabe
(DE-627)719034973
Eleya, Nadi Fakhry, 1978 -
urn:nbn:de:gbv:28-diss2012-0067-9
934783119
rakwb
DE-627
120906
723932565
20240716T195315.0
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