- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Expanding chemical space by para-C−H arylation of arenes ; volume:13 ; number:1 ; day:8 ; month:7 ; year:2022 ; pages:1-10 ; date:12.2022
Nature Communications ; 13, Heft 1 (8.7.2022), 1-10, 12.2022
- Creator
-
Maiti, Sudip
Li, Yingzi
Sasmal, Sheuli
Guin, Srimanta
Bhattacharya, Trisha
Lahiri, Goutam Kumar
Paton, Robert S.
Maiti, Debabrata
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-022-31506-x
- URN
-
urn:nbn:de:101:1-2022111309021984795659
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:27 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Maiti, Sudip
- Li, Yingzi
- Sasmal, Sheuli
- Guin, Srimanta
- Bhattacharya, Trisha
- Lahiri, Goutam Kumar
- Paton, Robert S.
- Maiti, Debabrata
- SpringerLink (Online service)
Other Objects (12)
Author Correction: Expanding chemical space by para-C−H arylation of arenes
Palladium-Catalyzed Oxidative Arylation of ortho-Phenylcarbamates with Arenes
Expanding Chemical Space in the Synthesis of Gold Bipyramids
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Visible‐Light‐Mediated Photoredox‐Catalyzed N ‐Arylation of NH ‐Sulfoximines with Electron‐Rich Arenes
Expanding and understanding metabolite space
Stochastic diffusion within expanding space–time
Modern arylation methods
Expanding the parameter space of natural supersymmetry
Author Correction: Expanding chemical space by para-C−H arylation of arenes
Palladium-Catalyzed Oxidative Arylation of ortho-Phenylcarbamates with Arenes
Expanding Chemical Space in the Synthesis of Gold Bipyramids
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Visible‐Light‐Mediated Photoredox‐Catalyzed N ‐Arylation of NH ‐Sulfoximines with Electron‐Rich Arenes
Expanding and understanding metabolite space
Stochastic diffusion within expanding space–time
Modern arylation methods
Expanding the parameter space of natural supersymmetry
Author Correction: Expanding chemical space by para-C−H arylation of arenes
Palladium-Catalyzed Oxidative Arylation of ortho-Phenylcarbamates with Arenes
Expanding Chemical Space in the Synthesis of Gold Bipyramids
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Ligand‐Enabled Nondirected and Regioselective Arylation of Internal Alkenes with Simple Arenes
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
Visible‐Light‐Mediated Photoredox‐Catalyzed N ‐Arylation of NH ‐Sulfoximines with Electron‐Rich Arenes
Expanding and understanding metabolite space
Stochastic diffusion within expanding space–time
Modern arylation methods