@article{oai:nagoya.repo.nii.ac.jp:00023506,
 author = {Nakazaki, Atsuo and Mori, Ayako and Kobayashi, Susumu and Nishikawa, Toshio},
 issue = {22},
 journal = {Chemistry-An Asian Journal},
 month = {Nov},
 note = {3,3-Disubstituted oxindoles were divergently synthesized by diastereoselective transformations including nucleophilic addition, alkylation, and cycloaddition using common, axially chiral N-aryl oxindoles. Notably, high diastereoselectivities (up to >95:5) were observed with ortho-monosubstituted N-aryl oxindoles to give various oxindole scaffolds, and facile removal of the p-(benzyloxy)aryl moiety in axially twisted amides was achieved by a mild, two-step sequence.},
 pages = {3267--3274},
 title = {A Divergent Approach to the Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives},
 volume = {11},
 year = {2016}
}