TY - JOUR
T1 - Photo-induced glycosylation using edible polyphenol ellagic acid
AU - Shigeta, Hidenari
AU - Goi, Satomi
AU - Takahashi, Daisuke
AU - Toshima, Kazunobu
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/6
Y1 - 2025/6
N2 - Photo-induced glycosylation reactions of trichloroacetoimidate donors with alcohol acceptors were investigated under visible light (470 nm) irradiation using the edible polyphenol, ellagic acid. We found, for the first time, that these glycosylations proceeded smoothly under mild reaction conditions, and the corresponding glycosides were obtained in high yields. Furthermore, this glycosylation method was applicable to a wide range of trichloroacetimidate donors and alcohol acceptors, and showed high chemoselectivity over glycosyl phosphate, fluoride, glycal, thioglycoside, and (N-phenyl)trifluoroacetimidate.
AB - Photo-induced glycosylation reactions of trichloroacetoimidate donors with alcohol acceptors were investigated under visible light (470 nm) irradiation using the edible polyphenol, ellagic acid. We found, for the first time, that these glycosylations proceeded smoothly under mild reaction conditions, and the corresponding glycosides were obtained in high yields. Furthermore, this glycosylation method was applicable to a wide range of trichloroacetimidate donors and alcohol acceptors, and showed high chemoselectivity over glycosyl phosphate, fluoride, glycal, thioglycoside, and (N-phenyl)trifluoroacetimidate.
KW - Edible polyphenol
KW - Ellagic acid
KW - Photo-induced glycosylation
UR - https://www.scopus.com/pages/publications/105000360715
UR - https://www.scopus.com/pages/publications/105000360715#tab=citedBy
U2 - 10.1016/j.carres.2025.109461
DO - 10.1016/j.carres.2025.109461
M3 - Article
C2 - 40120529
AN - SCOPUS:105000360715
SN - 0008-6215
VL - 552
JO - Carbohydrate Research
JF - Carbohydrate Research
M1 - 109461
ER -