Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group **
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group ** ; day:05 ; month:05 ; year:2022 ; extent:1
Angewandte Chemie ; (05.05.2022) (gesamt 1)
- Creator
-
Higham, Joe I.
Bull, James A.
- DOI
-
10.1002/ange.202202933
- URN
-
urn:nbn:de:101:1-2022050615205128273765
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 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
- Higham, Joe I.
- Bull, James A.
Other Objects (12)
Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group **
When is an Imine Directing Group a Transient Imine Directing Group in C−H Functionalization?
Palladium‐Catalyzed C (sp 3)−H Arylation of Primary Amines Using a Catalytic Alkyl Acetal to Form a Transient Directing Group
Ruthenium‐Catalyzed Deuteration of Aromatic Carbonyl Compounds with a Catalytic Transient Directing Group
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling
Palladium catalyzed ortho-C(sp2)–H activation/cyclization of aryl amines assisted by imine and vinylacetic acid
Insights into LiAlH4 Catalyzed Imine Hydrogenation
Imine-based dynamic polymer networks as photoprogrammable amine sensing devices
Magnesocenophane‐Catalyzed Amine Borane Dehydrocoupling
Actinomycetes-derived imine reductases with a preference towards bulky amine substrates
Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group **
When is an Imine Directing Group a Transient Imine Directing Group in C−H Functionalization?
Palladium‐Catalyzed C (sp 3)−H Arylation of Primary Amines Using a Catalytic Alkyl Acetal to Form a Transient Directing Group
Ruthenium‐Catalyzed Deuteration of Aromatic Carbonyl Compounds with a Catalytic Transient Directing Group
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling
Palladium catalyzed ortho-C(sp2)–H activation/cyclization of aryl amines assisted by imine and vinylacetic acid
Insights into LiAlH4 Catalyzed Imine Hydrogenation
Imine-based dynamic polymer networks as photoprogrammable amine sensing devices
Magnesocenophane‐Catalyzed Amine Borane Dehydrocoupling
Actinomycetes-derived imine reductases with a preference towards bulky amine substrates
Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group **
When is an Imine Directing Group a Transient Imine Directing Group in C−H Functionalization?
Palladium‐Catalyzed C (sp 3)−H Arylation of Primary Amines Using a Catalytic Alkyl Acetal to Form a Transient Directing Group
Ruthenium‐Catalyzed Deuteration of Aromatic Carbonyl Compounds with a Catalytic Transient Directing Group
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Pd II ‐Catalyzed C (alkenyl)−H Activation Facilitated by a Transient Directing Group **
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling
Palladium catalyzed ortho-C(sp2)–H activation/cyclization of aryl amines assisted by imine and vinylacetic acid
Insights into LiAlH4 Catalyzed Imine Hydrogenation
Imine-based dynamic polymer networks as photoprogrammable amine sensing devices
Magnesocenophane‐Catalyzed Amine Borane Dehydrocoupling