@article{oai:sucra.repo.nii.ac.jp:00012506,
 author = {松岡, 浩司 and 照沼, 大陽},
 issue = {8},
 journal = {Tetrahedron letters},
 month = {},
 note = {http://www.sciencedirect.com/science/journal/00404039 | http://www.sciencedirect.com/science/journal/00404039, A series of methylated b-cyclodextrins (CDs) regioselectively leaving one or two hydroxy groups were prepared, and fluorescence spectroscopic measurements showed that they have unique binding characteristics against 2-p-toluidinylnaphthalene-6-sulfonate as a guest molecule in aqueous solution., text, application/pdf},
 pages = {1531--1533},
 title = {Regioselective Synthesis of Methylated β-Cyclodextrins Leaving Hydroxy Groups},
 volume = {42},
 year = {2001},
 yomi = {マツオカ, コウジ and テルヌマ, ダイヨウ}
}