@article{oai:sucra.repo.nii.ac.jp:00012503,
 author = {松岡, 浩司 and 照沼, 大陽 and 幡野, 健},
 issue = {51},
 journal = {Tetrahedron letters},
 month = {},
 note = {http://www.sciencedirect.com/science/journal/00404039 | http://www.sciencedirect.com/science/journal/00404039, An efficient synthesis of a useful thioglycosyl donor 2 was accomplished directly from　known peracetylated sialic acid methyl ester and 1-dodecanethiol (lauryl mercaptan) in the presence of BF3—OEt2. The reactivities of the lauryl glycosides for glycosidation by means of TMSOTf as a convenient promoter were investigated, and　the lauryl thioglycoside showed satisfactory activities. Further transformation of the lauryl glycoside was also attempted to give a 5-azide analogue 14 of the sialic acid, which was also reacted with a secondary alcohol in the presence of TMSOTf to give known glycoside 15 in high yield., text, application/pdf},
 pages = {9383--9386},
 title = {Synthesis of a useful lauryl thioglycoside of sialic acid and its application},
 volume = {45},
 year = {2004},
 yomi = {マツオカ, コウジ and テルヌマ, ダイヨウ and ハタノ, ケン}
}