| Literature DB >> 33427338 |
Ana Koperniku1,2, Laurel L Schafer3.
Abstract
The zirconium catalyzed hydroaminoalkylation of alkenes with N-aryl- and sterically demanding N-alkyl-α-arylated secondary amines by using commercially available Zr(NMe2 )4 is reported. N-phenyl- and N-isopropylbenzylamine are used as amine substrates to establish the alkene substrate scope. Exclusively linear products are obtained in the presence of bulky vinylsilanes. Challenging α-heteroarylated amines and functionalized alkene substrates are compatible with this easy to use catalyst, affording a new disconnection strategy for the atom- and step-economic preparation of selectively substituted saturated α-arylated heterocycles.Entities:
Keywords: alpha-arylated amines; heterocycles; hydroaminoalkylation; zirconium
Year: 2021 PMID: 33427338 DOI: 10.1002/chem.202100014
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236