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- W2783178961 startingPage "3469" @default.
- W2783178961 abstract "Abstract Atom‐economic and regioselective C −C bond formation has been achieved by rapid C−H alkylation of unprotected secondary arylamines with unactivated alkenes. The combination of Ta(CH 2 SiMe 3 ) 3 Cl 2 , and a ureate N , O ‐chelating‐ligand salt gives catalytic systems prepared in situ that can realize high yields of β‐alkylated aniline derivatives from either terminal or internal alkene substrates. These new catalyst systems realize C−H alkylation in as little as one hour and for the first time a 1:1 stoichiometry of alkene and amine substrates results in high yielding syntheses of isolated amine products by simple filtration and concentration." @default.
- W2783178961 created "2018-01-26" @default.
- W2783178961 creator A5011354131 @default.
- W2783178961 creator A5019685588 @default.
- W2783178961 creator A5091821870 @default.
- W2783178961 date "2018-02-27" @default.
- W2783178961 modified "2023-10-16" @default.
- W2783178961 title "Catalytic and Atom‐Economic C−C Bond Formation: Alkyl Tantalum Ureates for Hydroaminoalkylation" @default.
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- W2783178961 doi "https://doi.org/10.1002/anie.201712668" @default.
- W2783178961 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29330909" @default.
- W2783178961 hasPublicationYear "2018" @default.
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