Synthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation Reactions

Ghazwan Ali Salman

doi:10.18453/rosdok_id00000983

Ghazwan Ali Salman

Synthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation Reactions

Universität Rostock, 2011

https://doi.org/10.18453/rosdok_id00000983

Abstract: The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions.

doctoral thesis free access

title:

Synthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation Reactions

contributing persons:

Ghazwan Ali Salman[VerfasserIn]
	1020214058
Peter Langer , Prof. Dr. Dr. h. c.[AkademischeR BetreuerIn]
Sabine Müller , Prof. Dr.[AkademischeR BetreuerIn]

contributing corporate bodies:

Universität Rostock, Mathematisch-Naturwissenschaftliche Fakultät[Grad-verleihende Institution]
	2147083-2

abstract:

The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions. [English]

document type:

doctoral thesis

institution:

Faculty of Mathematics and Natural Sciences

language:

English

subject class (DDC):

540 Chemistry & allied sciences

publication /
production:

Rostock

Rostock: Universität Rostock

2011