Dual Ligand-Enabled Nondirected C-H Cyanation of Arenes

Chen, Hao; Mondal, Arup; Wedi, Philipp; van Gemmeren, Manuel

doi:10.1021/acscatal.8b04639

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Dual Ligand-Enabled Nondirected C-H Cyanation of Arenes

MPS-Authors

/persons/resource/persons75360

Chen, Hao
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

/persons/resource/persons245025

Mondal, Arup
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

/persons/resource/persons237873

Wedi, Philipp
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

/persons/resource/persons58786

van Gemmeren, Manuel
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Chen, H., Mondal, A., Wedi, P., & van Gemmeren, M. (2019). Dual Ligand-Enabled Nondirected C-H Cyanation of Arenes. ACS Catalysis, 9(3), 1979-1984. doi:10.1021/acscatal.8b04639.

Cite as: https://hdl.handle.net/21.11116/0000-0005-A9F9-4

Abstract

Aromatic nitriles are key structural units in organic chemistry and, therefore, highly attractive targets for C-H activation. Herein, the development of an arene-limited, nondirected C-H cyanation based on the use of two cooperatively acting commercially available ligands is reported. The reaction enables the cyanation of arenes by C-H activation in the absence of directing groups and is therefore complementary to established approaches.