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
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
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
10.1002/chem.202003484
URN
urn:nbn:de:101:1-2022060417333253200932
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:31 AM CEST

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