@article{oai:oist.repo.nii.ac.jp:00001865,
 author = {Rahaman, S. M. Wahidur and Pandey, Dilip K. and Rivada‐Wheelaghan, Orestes and Dubey, Abhishek and Fayzullin, Robert R. and Khusnutdinova, Julia R.},
 issue = {23},
 journal = {ChemCatChem},
 month = {Oct},
 note = {Hydrogenation of substituted styrenes and unactivated aliphatic alkenes by molecular hydrogen has been achieved using a Mn catalyst with a non‐pincer, picolylphosphine ligand. This is the second reported example of alkene hydrogenation catalyzed by a Mn complex. Mechanistic studies showed that a Mn hydride formed by H2 activation in the presence of a base is the catalytically active species. Based on experimental and DFT studies, H2 splitting is proposed to occur via a metal‐ligand cooperative pathway involving deprotonation of the CH2 arm of the ligand, leading to pyridine dearomatization.},
 pages = {5912--5918},
 title = {Hydrogenation of Alkenes Catalyzed by a Non‐pincer Mn Complex},
 volume = {12},
 year = {2020}
}