Synthesis of functionalized isatins, benzoxazoles, isoflavones, coumarins, by site-selective Suzuki-Miyaura cross-coupling reactions
Al-Abo, Aws Mardan Hamdy
1975-
aut
text
theses
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Hochschulschrift
gw
2015
monographic
XA-DE
2015
eng
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This thesis includes regioselective palladium catalyzed Suzuki-Miyaura cross coupling reactions of isatins benzoxazols isoflavones and coumarins. These classes of compounds are of pharmacological relevance. Suzuki-Miyaura cross-coupling reactions of dichloro methylindolinen dione afforded arylated isatins. The reactions proceeded with very good site selectivity. The Suzuki-Miyaura reaction of dichlorobenzoxazol, of the bis(triflate) of dihydroxyisoflavone, and of the bis(triflate) of methyl dihydroxycoumarin, with different boronic acids, gave the corresponding site-selective mono-arylated, homo bis-arylated and mixed bis-arylated derivaties, most of them with very good site-selectivity.
vorgelegt von M.Sc. Aws Mardan Hamdy Al-Abo
Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2015
547.27
547.596
540
35.50
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0197-1
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0197-1&pdf
http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2015-0197-1
Synthesis of functionalized isatins, benzoxazoles, isoflavones, coumarins, by site-selective Suzuki-Miyaura cross-coupling reactions
2015
Druck-Ausgabe
(DE-627)838726631
Al-Abo, Aws Mardan Hamdy, 1975 -
urn:nbn:de:gbv:28-diss2015-0197-1
935976162
rakwb
DE-627
151208
842372172
20251224T201011.0
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