ChemInform Abstract: Combined Metalation-Palladium-Catalyzed Cross Coupling Strategies. A Formal Synthesis of the Marine Alkaloid Amphimedine.

ChemInform ◽  
2010 ◽  
Vol 26 (30) ◽  
pp. no-no
Author(s):  
F. GUILLIER ◽  
F. NIVOLIERS ◽  
A. GODARD ◽  
F. MARSAIS ◽  
G. QUEGUINER ◽  
...  
1995 ◽  
Vol 60 (2) ◽  
pp. 292-296 ◽  
Author(s):  
F. Guillier ◽  
F. Nivoliers ◽  
A. Godard ◽  
F. Marsais ◽  
G. Queguiner ◽  
...  

2019 ◽  
Vol 2019 (19) ◽  
pp. 3022-3034 ◽  
Author(s):  
Alessandra A. G. Fernandes ◽  
Amanda F. da Silva ◽  
Celso Y. Okada ◽  
Vitor Suzukawa ◽  
Rodrigo A. Cormanich ◽  
...  

1999 ◽  
Vol 40 (26) ◽  
pp. 4769-4773 ◽  
Author(s):  
Devan Balachari ◽  
Liam Quinn ◽  
George A. O'Doherty

2020 ◽  
Author(s):  
Jian Cao ◽  
Ernest Armenta ◽  
Lisa Boatner ◽  
Heta Desai ◽  
Neil Chan ◽  
...  

Bioorthogonal chemistry is a mainstay of chemoproteomic sample preparation workflows. While numerous transformations are now available, chemoproteomic studies still rely overwhelmingly on copper-catalyzed azide –alkyne cycloaddition (CuAAC) or 'click' chemistry. Here we demonstrate that gel-based activity-based protein profiling (ABPP) and mass-spectrometry-based chemoproteomic profiling can be conducted using Suzuki–Miyaura cross-coupling. We identify reaction conditions that proceed in complex cell lysates and find that Suzuki –Miyaura cross-coupling and CuAAC yield comparable chemoproteomic coverage. Importantly, Suzuki–Miyaura is also compatible with chemoproteomic target deconvolution, as demonstrated using structurally matched probes tailored to react with the cysteine protease caspase-8. Uniquely enabled by the observed orthogonality of palladium-catalyzed cross-coupling and CuAAC, we combine both reactions to achieve dual protein labeling.


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