Effective and Variable Functionalization of Pyrazolo[1,5-a]pyridines Involving Palladium-Catalyzed Coupling Reactions

Löber S, Gmeiner P (2000)

Publication Type: Journal article

Publication year: 2000

Journal

Synthesis-Stuttgart Thieme Publishing / Georg Thieme Verlag

Publisher: Thieme Publishing / Georg Thieme Verlag

Pages Range: 1727-1732

DOI: 10.1055/s-2000-8215

Abstract

Various 7-substituted pyrazolo[1,5-a]pyridines were synthesized by palladium-mediated cross-coupling reactions. Starting from the corresponding 7-iodo derivatives, incorporation of phenyl, vinyl, ethynyl, cyano, and amino was accomplished. Pyrazolo[1,5-a]pyridine-7-ylzinc iodide could be reacted under Negishi conditions to afford the coupling product 16.

Authors with CRIS profile

Stefan Löber Lehrstuhl für Pharmazeutische Chemie Peter Gmeiner Lehrstuhl für Pharmazeutische Chemie

How to cite

APA:

Löber, S., & Gmeiner, P. (2000). Effective and Variable Functionalization of Pyrazolo[1,5-a]pyridines Involving Palladium-Catalyzed Coupling Reactions. Synthesis-Stuttgart, 1727-1732. https://doi.org/10.1055/s-2000-8215

MLA:

Löber, Stefan, and Peter Gmeiner. "Effective and Variable Functionalization of Pyrazolo[1,5-a]pyridines Involving Palladium-Catalyzed Coupling Reactions." Synthesis-Stuttgart (2000): 1727-1732.

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