Bridging and Conformational Control of Porphyrin Units through Non‐Traditional Rigid Scaffolds
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Bridging and Conformational Control of Porphyrin Units through Non‐Traditional Rigid Scaffolds ; volume:26 ; number:11 ; year:2020 ; pages:2405-2416 ; extent:12
Chemistry - a European journal ; 26, Heft 11 (2020), 2405-2416 (gesamt 12)
- Creator
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Grover, Nitika
Locke, Gemma M.
Flanagan, Keith J.
Beh, Michael H. R.
Thompson, Alison
Senge, Mathias O.
- DOI
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10.1002/chem.201904199
- URN
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urn:nbn:de:101:1-2022060713591087452118
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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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
- Grover, Nitika
- Locke, Gemma M.
- Flanagan, Keith J.
- Beh, Michael H. R.
- Thompson, Alison
- Senge, Mathias O.
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The Active Site of a Prototypical “Rigid” Drug Target is Marked by Extensive Conformational Dynamics
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Identification of “Structural Pin” Interactions and their Significance for the Conformational Control of Macrocyclic Scaffolds
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Rigid Scaffolds: Synthesis of 2,6‐Bridged Piperazines with Functional Groups in all three Bridges
Rigid Scaffolds: Synthesis of 2,6-Bridged Piperazines with Functional Groups in all three Bridges
Conformational switching of ethano-bridged Cu,H2-bis-porphyrin induced by aromatic amines
Tetrachromophoric Systems Based On Rigid Tetraphenylmethane (TPM) and Tetraphenylethylene (TPE) Scaffolds
Porphyrin-Isomere
The Active Site of a Prototypical “Rigid” Drug Target is Marked by Extensive Conformational Dynamics
The Active Site of a Prototypical “Rigid” Drug Target is Marked by Extensive Conformational Dynamics
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Critical challenges and barriers to online learning : nontraditional adult students in a nontraditional teacher licensing program
Identification of “Structural Pin” Interactions and their Significance for the Conformational Control of Macrocyclic Scaffolds
Identification of “Structural Pin” Interactions and their Significance for the Conformational Control of Macrocyclic Scaffolds
Rigid Scaffolds: Synthesis of 2,6‐Bridged Piperazines with Functional Groups in all three Bridges
Rigid Scaffolds: Synthesis of 2,6-Bridged Piperazines with Functional Groups in all three Bridges
Conformational switching of ethano-bridged Cu,H2-bis-porphyrin induced by aromatic amines
Tetrachromophoric Systems Based On Rigid Tetraphenylmethane (TPM) and Tetraphenylethylene (TPE) Scaffolds
Porphyrin-Isomere
The Active Site of a Prototypical “Rigid” Drug Target is Marked by Extensive Conformational Dynamics
The Active Site of a Prototypical “Rigid” Drug Target is Marked by Extensive Conformational Dynamics
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Critical challenges and barriers to online learning : nontraditional adult students in a nontraditional teacher licensing program
Identification of “Structural Pin” Interactions and their Significance for the Conformational Control of Macrocyclic Scaffolds
Identification of “Structural Pin” Interactions and their Significance for the Conformational Control of Macrocyclic Scaffolds
Rigid Scaffolds: Synthesis of 2,6‐Bridged Piperazines with Functional Groups in all three Bridges