@article{oai:nagasaki-u.repo.nii.ac.jp:00010551,
 author = {Mizuta, Satoshi and Onomura, Osamu},
 issue = {6},
 journal = {RSC Advances},
 month = {Mar},
 note = {A highly diastereoselective synthesis of 2,3-disubstituted piperidines has been accomplished through nucleophilic additions to N-acyliminium ions with aryl- and alkenyl boronic acids. A reversal of stereoselectivity depending on a β-substituent on the piperidine ring was observed in the alkenylation reactions with (E)-styrylboronic acid. Our strategy was applied in the key step for the synthesis of the neurokinin NK1 receptor antagonist (±)-L-733, 060., RSC Advances, 2(6), pp.2266-2269; 2012},
 pages = {2266--2269},
 title = {Diastereoselective addition to N-acyliminium ions with aryl- and alkenyl boronic acids via a Petasis-type reaction},
 volume = {2},
 year = {2012}
}