@article{oai:kanagawa-u.repo.nii.ac.jp:00002950,
 author = {安盛, 俊雄 and Yasumori, Toshio and 佐藤, 憲一 and Sato, Ken-ichi and 橋本, 弘信 and Hashimoto, Hironobu and 吉村, 寿次 and Yoshimura, Juji},
 issue = {9},
 journal = {Bulletin of the Chemical Society of Japan},
 month = {Sep},
 note = {The title compound was synthesized from methyl 4-O-benzyl-2,6-dideoxy-β-L-threo-hexopyranosid-3-ulose (19) through cyanomesylation, reductive spiro aziridine formation, and reductive ring-opening. When (2-methoxyethoxymethyl) group was used as the protecting group at O-4 of the above intermediate, it could not be removed at the final stage., Article},
 pages = {2538--2542},
 title = {Branched-chain Sugars. XXXVI. A New Synthesis of Methyl 4-O-Benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside, a Derivative of the Branched-chain Amino Sugar of Antibiotic A35512B},
 volume = {57},
 year = {1984}
}