@article{oai:soar-ir.repo.nii.ac.jp:00017862,
 author = {Kitajima,  Kai and Nagatomo,  Ryota and Fujimoto,  Tetsuya},
 issue = {6},
 journal = {TETRAHEDRON},
 month = {Feb},
 note = {The reaction of chiral imines, derived from aromatic aldehydes and (S)-valinol, with a Grignard reagent in the presence of Mg(0) afforded imino-pinacol coupling products instead of alkylated amines, with a high level of diastereoselectivity. The chiral auxiliary in the product was successfully removed via dehydration followed by hydrolysis, and the corresponding (R,R)-ethylenediamine derivative was obtained as the N-Boc protected form. (C) 2014 Elsevier Ltd. All rights reserved., Article, TETRAHEDRON. 71(6):977-981 (2015)},
 pages = {977--981},
 title = {Diastereoselective imino-pinacol coupling of chiral imines promoted by Mg(0) and a Grignard reagent},
 volume = {71},
 year = {2015}
}