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
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