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Chemo-Enzymatic Synthesis of 1’-Photoreactive Sucrose Derivatives via Ether Linkage

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/51766

Title: Chemo-Enzymatic Synthesis of 1’-Photoreactive Sucrose Derivatives via Ether Linkage
Authors: Tsunekawa, Yuka Browse this author
Masuda, Katsuyoshi Browse this author →KAKEN DB
Muto, Miho Browse this author
Muto, Yasuyuki Browse this author
Murai, Yuta Browse this author
Hashidoko, Yasuyuki Browse this author →KAKEN DB
Orikasa, Yoshitake Browse this author
Oda, Yuji Browse this author →KAKEN DB
Hatanaka, Yasumaru Browse this author →KAKEN DB
Hashimoto, Makoto Browse this author →KAKEN DB
Keywords: sucrose
photoaffinity label
diazirine
Mitsunobu reaction
sweet receptor
Issue Date: 2012
Publisher: The Japan Institute of Heterocyclic Chemistry
Journal Title: HETEROCYCLES
Volume: 84
Issue: 1
Start Page: 283
End Page: 290
Publisher DOI: 10.3987/COM-11-S(P)19
Abstract: As the 1’-hydroxyl group of sucrose is well known to be less reactive than other primary alcohols, there are no reports on the substitution of a phenoxy group at this position. Chemo-enzymatic synthesis of photoreactive 1’-phenoxy-substituted sucrose was examined to elucidate the functional analysis of sweet receptors.
Type: article (author version)
URI: http://hdl.handle.net/2115/51766
Appears in Collections:農学院・農学研究院 (Graduate School of Agriculture / Faculty of Agriculture) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 橋本 誠

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