Electrochemical Proton Reduction over Nickel Foam for Z ‐Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Electrochemical Proton Reduction over Nickel Foam for Z ‐Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes ; day:16 ; month:12 ; year:2021 ; extent:1
ChemSusChem ; (16.12.2021) (gesamt 1)
- Urheber
-
Valiente, Alejandro
Martínez‐Pardo, Pablo
Kaur, Gurpreet
Johansson, Magnus J.
Martín‐Matute, Belén
- DOI
-
10.1002/cssc.202102221
- URN
-
urn:nbn:de:101:1-2021121714162905611362
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Valiente, Alejandro
- Martínez‐Pardo, Pablo
- Kaur, Gurpreet
- Johansson, Magnus J.
- Martín‐Matute, Belén
Ähnliche Objekte (12)
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Stereoselective Chromium‐Catalyzed Semi‐Hydrogenation of Alkynes
Electrochemical Hydroboration of Alkynes
Regio- and stereoselective catalytic addition of amides to alkynes
Gold-Catalyzed Regio- and Stereoselective Acyloxyalkynylations and Cycloadditions of Alkynes
New Methodologies for the Regio- and Stereoselective Electrophilic Cyanation of Alkynes
E ‐Selective Radical Difunctionalization of Unactivated Alkynes: Preparation of Functionalized Allyl Alcohols from Aliphatic Alkynes
Functionalized Molecular Diversity by Gold-Catalyzed Activation of Alkynes
Stereoselective Semi‐Hydrogenations of Alkynes by First‐Row (3d) Transition Metal Catalysts
Ligand-functionalized nanoparticles for chemo- and stereoselective, heterogeneous catalysis
Highly regio- and stereoselective phosphinylphosphination of terminal alkynes with tetraphenyldiphosphine monoxide under radical conditions
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Stereoselective Chromium‐Catalyzed Semi‐Hydrogenation of Alkynes
Electrochemical Hydroboration of Alkynes
Regio- and stereoselective catalytic addition of amides to alkynes
Gold-Catalyzed Regio- and Stereoselective Acyloxyalkynylations and Cycloadditions of Alkynes
New Methodologies for the Regio- and Stereoselective Electrophilic Cyanation of Alkynes
E ‐Selective Radical Difunctionalization of Unactivated Alkynes: Preparation of Functionalized Allyl Alcohols from Aliphatic Alkynes
Functionalized Molecular Diversity by Gold-Catalyzed Activation of Alkynes
Stereoselective Semi‐Hydrogenations of Alkynes by First‐Row (3d) Transition Metal Catalysts
Ligand-functionalized nanoparticles for chemo- and stereoselective, heterogeneous catalysis
Highly regio- and stereoselective phosphinylphosphination of terminal alkynes with tetraphenyldiphosphine monoxide under radical conditions
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Silver‐Catalyzed Stereoselective Aminosulfonylation of Alkynes
Stereoselective Chromium‐Catalyzed Semi‐Hydrogenation of Alkynes
Electrochemical Hydroboration of Alkynes
Regio- and stereoselective catalytic addition of amides to alkynes
Gold-Catalyzed Regio- and Stereoselective Acyloxyalkynylations and Cycloadditions of Alkynes
New Methodologies for the Regio- and Stereoselective Electrophilic Cyanation of Alkynes
E ‐Selective Radical Difunctionalization of Unactivated Alkynes: Preparation of Functionalized Allyl Alcohols from Aliphatic Alkynes
Functionalized Molecular Diversity by Gold-Catalyzed Activation of Alkynes
Stereoselective Semi‐Hydrogenations of Alkynes by First‐Row (3d) Transition Metal Catalysts
Ligand-functionalized nanoparticles for chemo- and stereoselective, heterogeneous catalysis