Enhancing Auxiliary‐Mediated Native Chemical Ligation at Challenging Junctions with Pyridine Scaffolds
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
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Enhancing Auxiliary‐Mediated Native Chemical Ligation at Challenging Junctions with Pyridine Scaffolds ; day:17 ; month:10 ; year:2022 ; extent:1
Chemistry - a European journal ; (17.10.2022) (gesamt 1)
- Creator
- DOI
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10.1002/chem.202202065
- URN
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urn:nbn:de:101:1-2022101815444521126533
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 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
- Trunschke, Sebastian
- Piemontese, Emanuele
- Fuchs, Olaf
- Abboud, Skander
- Seitz, Oliver
Other Objects (12)
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Enabling Cysteine-Free Native Chemical Ligation at Challenging Junctions with a Ligation Auxiliary Capable of Base Catalysis
Extending the scope of protein synthesis by a novel auxiliary‐based native chemical ligation strategy
Elucidation of Switching Mechanisms in Memristive Junctions Integrating a Iron (II)‐Ter Pyridine Diazoted Complex
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Discovering the stacking landscape of a pyridine-pyridine system
Hydrogen Bonding, π‐Stacking, and Aurophilic Interactions in Two Dicyanoaurate (I)‐Based Manganese (II) Complexes with Auxiliary Bis‐Pyridine Ligands
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Hydroboration with Pyridine Borane
Enhancing Auxiliary-Mediated Native Chemical Ligation at Challenging Junctions with Pyridine Scaffolds
Enabling Cysteine‐Free Native Chemical Ligation at Challenging Junctions with a Ligation Auxiliary Capable of Base Catalysis
Enabling Cysteine-Free Native Chemical Ligation at Challenging Junctions with a Ligation Auxiliary Capable of Base Catalysis
Extending the scope of protein synthesis by a novel auxiliary‐based native chemical ligation strategy
Elucidation of Switching Mechanisms in Memristive Junctions Integrating a Iron (II)‐Ter Pyridine Diazoted Complex
Auxiliary Verbs.
Verbs, Auxiliary
Discovering the stacking landscape of a pyridine-pyridine system
Hydrogen Bonding, π‐Stacking, and Aurophilic Interactions in Two Dicyanoaurate (I)‐Based Manganese (II) Complexes with Auxiliary Bis‐Pyridine Ligands
Ladies' Auxiliary news
Govindpur Auxiliary File
Hydroboration with Pyridine Borane
Enhancing Auxiliary-Mediated Native Chemical Ligation at Challenging Junctions with Pyridine Scaffolds
Enabling Cysteine‐Free Native Chemical Ligation at Challenging Junctions with a Ligation Auxiliary Capable of Base Catalysis
Enabling Cysteine-Free Native Chemical Ligation at Challenging Junctions with a Ligation Auxiliary Capable of Base Catalysis
Extending the scope of protein synthesis by a novel auxiliary‐based native chemical ligation strategy
Elucidation of Switching Mechanisms in Memristive Junctions Integrating a Iron (II)‐Ter Pyridine Diazoted Complex
Auxiliary Verbs.
Verbs, Auxiliary
Discovering the stacking landscape of a pyridine-pyridine system
Hydrogen Bonding, π‐Stacking, and Aurophilic Interactions in Two Dicyanoaurate (I)‐Based Manganese (II) Complexes with Auxiliary Bis‐Pyridine Ligands
Ladies' Auxiliary news
Govindpur Auxiliary File