Synthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactions

Ali Asad

doi:10.18453/rosdok_id00000733

Ali Asad

Synthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactions

Universität Rostock, 2010

https://doi.org/10.18453/rosdok_id00000733

Abstract: Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.

doctoral thesis free access

title:

Synthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactions

contributing persons:

Ali Asad[VerfasserIn]
	142870900
Peter Langer , Prof. Dr.[AkademischeR BetreuerIn]
Andreas Kirschning , Prof. Dr.[AkademischeR BetreuerIn]

contributing corporate bodies:

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

abstract:

Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products. [German]

document type:

doctoral thesis

institution:

Faculty of Mathematics and Natural Sciences

language:

English

subject class (DDC):

540 Chemistry & allied sciences

publication /
production:

Rostock: Universität Rostock

2010

identifiers: