Author Correction: Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Author Correction: Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids ; volume:15 ; number:1 ; day:28 ; month:2 ; year:2024 ; pages:1 ; date:12.2024
Nature Communications ; 15, Heft 1 (28.2.2024), 1, 12.2024
- Creator
-
Xu, Fang-Fang
Chen, Jin-Quan
Shao, Dong-Yang
Huang, Pei-Qiang
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-024-46252-5
- URN
-
urn:nbn:de:101:1-2405061033149.579832821892
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
2025-08-14T10:50:59+0200
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
- Xu, Fang-Fang
- Chen, Jin-Quan
- Shao, Dong-Yang
- Huang, Pei-Qiang
- SpringerLink (Online service)
Other Objects (12)
Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids
Enantioselective synthesis of γ-chiral amides via copper-catalyzed reductive relay hydroaminocarbonylation
Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses
Ruthenium-Catalyzed Enantioselective Reductive Amination
Nickel-Catalyzed Enantioselective Reductive Diarylation
Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines
Iridium-catalyzed reductive Ugi-type reactions of tertiary amides
Enantioselective Syntheses of π-Extended Carbohelicenes
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling
Multicomponent and One‐pot Syntheses of Quinoxalines
Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids
Enantioselective synthesis of γ-chiral amides via copper-catalyzed reductive relay hydroaminocarbonylation
Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses
Ruthenium-Catalyzed Enantioselective Reductive Amination
Nickel-Catalyzed Enantioselective Reductive Diarylation
Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines
Iridium-catalyzed reductive Ugi-type reactions of tertiary amides
Enantioselective Syntheses of π-Extended Carbohelicenes
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling
Multicomponent and One‐pot Syntheses of Quinoxalines
Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids
Enantioselective synthesis of γ-chiral amides via copper-catalyzed reductive relay hydroaminocarbonylation
Lewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses
Ruthenium-Catalyzed Enantioselective Reductive Amination
Nickel-Catalyzed Enantioselective Reductive Diarylation
Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines
Iridium-catalyzed reductive Ugi-type reactions of tertiary amides
Enantioselective Syntheses of π-Extended Carbohelicenes
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
One‐Pot Transition‐Metal‐Free Synthesis of Alkynyl Amides
Iridium-Catalyzed Enantioselective Alkyne-Imine Reductive Coupling