2026-03-14T16:51:05Z https://kait.repo.nii.ac.jp/oai

oai:kait.repo.nii.ac.jp:00012104 2025-07-04T06:18:55Z 2:16:43:192

L -アスコルビン酸とフェニルボロン酸との反応挙動の評価 Study on the reaction behavior of L-ascorbic acid and phenylboronic acid 武田, 唯子 Takeda, Yuiko 森川, 浩 Morikawa, Hiroshi L-Ascorbic acid Phenylboronic acid Ester Reaction behavior Diol application/pdf This study shows reaction behavior of L-ascorbic acid (AA) and phenylboronic acid (PB) in DMSO-d6 (50 mM at 30oC) to form the corresponding boronic acid ester. For the purpose of restriction of the reactive moieties, two AA derivatives, in which diols at 2,3- or 5,6-position are protected, were selected and evaluated as the reference for AA. Compared among their 1H NMR spectra of the boronic acid ester from the protected AA with PB, unmodified AA was reacted with PB mainly at not the 2,3-position but the 5,6-position of AA. When equimolar AA and PB were mixed in DMSO-d6, it was found that approximately a half of AA was converted to the boronic acid ester. departmental bulletin paper 神奈川工科大学 2020-03-01 VoR application/pdf 神奈川工科大学研究報告.B,理工学編 44 61 64 AA12669200 21882878 https://kait.repo.nii.ac.jp/record/12104/files/kkb-044-010.pdf https://doi.org/10.34411/00032032 http://hdl.handle.net/10368/00032032 https://kait.repo.nii.ac.jp/records/12104 jpn