New palladium(0)-catalyzed reactions of 2,3-dibromobenzofuran, 2,3,5-tribromobenzofuran, and 2,3-dibromoindenone
Nguyen, Thai Hung
1976-
aut
text
theses
Text
Hochschulschrift
gw
2010
monographic
XA-DE
2010
eng
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application/pdf
Online-Ressource graph. Darst.
Functionalized dibenzofurans were prepared based on domino twofold Heck / 6-electrocyclization reactions of 2,3-di- and 2,3,5-tribromobenzofuran. The SuzukiMiyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from in a one-pot protocol. The Suzuki-Miyaura reaction of 2,3-dibromo-1H-inden-1-one with one equivalent of arylboronic acid gave 2-bromo-3-aryl-1H-inden-1-ones with very good site-selectivity. The one-pot reaction also afforded 2,3-diaryl-1H-inden-1-ones containing two different terminal aryl groups.
vorgelegt von Nguyen Thai Hung
Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2011
540
35.69
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2011-0102-7
http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2011-0102-7&pdf
http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2011-0102-7
New palladium(0)-catalyzed reactions of 2,3-dibromobenzofuran, 2,3,5-tribromobenzofuran, and 2,3-dibromoindenone
2010
Druck-Ausgabe
(DE-627)663631874
Nguyen, Thai Hung, 1976 -
urn:nbn:de:gbv:28-diss2011-0102-7
838181593
rakwb
DE-627
110722
66467495X
20251223T225825.0
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