@article{oai:nagoya.repo.nii.ac.jp:02002062,
 author = {Shibuya, Masatoshi and Orihashi, Takayuki and Li, Yamei and Yamamoto, Yoshihiko},
 journal = {Chemical Communications},
 month = {Sep},
 note = {N-Hydroxyphthalimide-catalyzed chemoselective benzylic C(sp^3)–H amination of unprotected arylalkanols using bis(2,2,2-trichloroethyl)azodicarboxylate has been developed. The use of 1,1,1,3,3,3-hexafluoropropan-2-ol as a solvent plays a critical role in chemoselectivity. The conversion of an aminated product to the corresponding free amino alcohol was also demonstrated.},
 pages = {8742--8745},
 title = {N-Hydroxyphthalimide-catalyzed chemoselective intermolecular benzylic C–H amination of unprotected arylalkanols},
 volume = {57},
 year = {2021}
}