@article{oai:nagasaki-u.repo.nii.ac.jp:00020380,
 author = {Onomura, Osamu and Kouchi, Yoshimi and Iwasaki, Fumiaki and Matsumura, Yoshihiro},
 issue = {22},
 journal = {Tetrahedron Letters},
 month = {May},
 note = {N-Picolinoyl-(2S)-(diphenylhydroxymethyl)pyrrolidine was found to work as an organic activator in the reduction of aromatic imines to the corresponding amines by Cl3SiH. The highest selectivity was 80% ee. These are the first data showing that N-formyl group is not always essential as N-protecting group of pyrrolidine derivatives for the reduction of imines by Cl3SiH., Tetrahedron Letters 47(22) pp.3751-3754, 2006},
 pages = {3751--3754},
 title = {New organic activators for the enantioselective reduction of aromatic imines with trichlorosilane},
 volume = {47},
 year = {2006}
}