Autor: |
Su, Jianhong, Luo, Yuncong, Xu, Xin |
Předmět: |
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Zdroj: |
Chemical Communications; 4/18/2021, Vol. 57 Issue 30, p3688-3691, 4p |
Abstrakt: |
An efficient and selective benzylic C(sp3)–H addition of o-CH3-substituted tertiary aromatic amines to alkenes has been achieved using an anilido-oxazoline ligand supported scandium catalyst, which provides an atom-economic method for the synthesis of a new family of alkylated tertiary anilines. A wide range of amine and alkene substrates are compatible with the catalyst system. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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