@article{oai:kanazawa-u.repo.nii.ac.jp:00011066,
 author = {Kometani, Miki and Ihara, Kohei and Kimura, Rumi and Kinoshita, Hideki},
 issue = {3},
 journal = {Bulletin of the Chemical Society of Japan},
 month = {Jan},
 note = {Reaction of methyl N-Boc-N-phenoxycarbonylglycinate with various aldehydes afforded the corresponding cis-4,5-oxazolidinone derivatives, which were effectively converted to (E)-α,β-didehydroamino acids by means of a base. Furthermore, N-deprotection of the oxazolidinone derivatives and subsequent coupling reaction with Boc-amino acid furnished the corresponding dipeptides, which were transformed to dipeptide containing α,β-didehydroamino acid with high E selectivity., 金沢大学理工学域},
 pages = {364--380},
 title = {Stereoselective syntheses of (E)-α,β-didehydroamino acid and peptide containing its residue utilizing oxazolidinone derivative},
 volume = {82},
 year = {2009}
}