writer：Guodu Liu, Zhao Li, Huiling Geng,* Xumu Zhang.*
keywords：regioselective hydroaminomethylation
source：期刊
specific source：Catal. Sci. Technol. 2014, 4, 917-921. (DOI: 10.1039/C3CY01069D, communication, IF = 5.726, Citation
Issue time：2014年

A concise and elegant protocol was developed to prepare linear amines by regioselective hydroaminomethylation of terminal olefins with pyrrole-based tetraphosphorus ligands. It has been documented that the reactivity of the ligand is modulated by the substituent of the 

biphenylphosphane moiety. Ligand L5 containing electron-donating groups exhibited the highest reactivity, with up to 70.9 n/i ratio and 99.5% amine selectivity for 1-pentene and a 31.3 n/i ratio and 97.9% amine selectivity for 1-hexene.