@article{oai:sucra.repo.nii.ac.jp:00012487,
 author = {松岡, 浩司 and 照沼, 大陽 and 幡野, 健},
 issue = {18},
 journal = {Tetrahedron letters},
 month = {},
 note = {http://www.sciencedirect.com/science/journal/00404039 | http://www.sciencedirect.com/science/journal/00404039, A novel anomeric b-thioacetate of an N-acetyllactosamine derivative was efficiently synthesized in high yield from the known 2-azido glycosyl chloride using thioacetic acid as a convenient reagent.  The synthesis involved not only an SN2 replacement of the chloride by a carbothiolate anion but also a reductive acetamidation of the azide group.  Applications of the thioacetate for glycosidation were demonstrated to provide both O- and S-glycosides in high yields.  Furthermore, both intermediates gave a new class of glycoclusters that included thioglycosidic linkages., text, application/pdf},
 title = {Synthesis of a useful anomeric thioacetate of an N-acetyllactosamine derivative and its application},
 volume = {44},
 year = {2003},
 yomi = {マツオカ, コウジ and テルヌマ, ダイヨウ and ハタノ, ケン}
}