Intermolecular Hydroaminoalkylation of Propadiene
Abstract: Intermolecular hydroaminoalkylation reactions of propadiene with selected secondary amines take place in the presence of a 2,6‐bis (phenylamino) pyridinato titanium catalyst. The corresponding products, synthetically useful allylamines, are formed in convincing yields and with high selectivities. In addition, propadiene easily inserts into the titanium‐carbon bond of a titanaaziridine.
- 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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Intermolecular Hydroaminoalkylation of Propadiene ; volume:26 ; number:63 ; year:2020 ; pages:14300-14304 ; extent:5
Chemistry - a European journal ; 26, Heft 63 (2020), 14300-14304 (gesamt 5)
- Creator
- DOI
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10.1002/chem.202003484
- URN
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urn:nbn:de:101:1-2022060417333253200932
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:31 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
- Kaper, Tobias
- Fischer, Malte
- Warsitz, Michael
- Zimmering, René
- Beckhaus, Rüdiger
- Doye, Sven
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