- 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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Nickel-Catalyzed Asymmetric Reductive Coupling of Vinyl and Benzyl Halides ; volume:11 ; number:01 ; year:2015 ; pages:0058-0058
Synfacts ; 11, Heft 01 (2015), 0058-0058
- DOI
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10.1055/s-0034-1379687
- URN
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urn:nbn:de:101:1-2019030814570365945257
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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2025-08-14T10:55:49+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.
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Visible light mediated activation of vinyl halides
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Nickel-Catalyzed Enantioselective Reductive Diarylation
Stereospecific Nickel-Catalyzed Borylation of Secondary Benzyl Pivalates
Nickel‐Catalyzed Reductive Hydrolysis of Nitriles to Alcohols
Nickel‐Catalyzed Reductive Hydrolysis of Nitriles to Alcohols
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Regiocontrol in the Nickel-Catalyzed Aldehyde-Alkyne Reductive Coupling
Nickel-Catalyzed Reductive Carboxylation of Cyclopropyl Motifs with Carbon Dioxide
Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
Visible light mediated activation of vinyl halides
Nickel-catalyzed selective disulfide formation by reductive cross-coupling of thiosulfonates
Intermolecular selective carboacylation of alkenes via nickel-catalyzed reductive radical relay
Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides
Nickel-Catalyzed Enantioselective Reductive Diarylation
Stereospecific Nickel-Catalyzed Borylation of Secondary Benzyl Pivalates
Nickel‐Catalyzed Reductive Hydrolysis of Nitriles to Alcohols
Nickel‐Catalyzed Reductive Hydrolysis of Nitriles to Alcohols
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Regiocontrol in the Nickel-Catalyzed Aldehyde-Alkyne Reductive Coupling
Nickel-Catalyzed Reductive Carboxylation of Cyclopropyl Motifs with Carbon Dioxide
Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
Visible light mediated activation of vinyl halides
Nickel-catalyzed selective disulfide formation by reductive cross-coupling of thiosulfonates