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Radical C-Glycosylation Using Photoexcitable Unprotected Glycosyl Borate.
Miyamoto, Yusuke; Murakami, Sho; Sumida, Yuto; Hirai, Go; Ohmiya, Hirohisa.
Affiliation
  • Miyamoto Y; Institute for Chemical Research Kyoto University, 611-0011, Gokasho, Uji, Kyoto, Japan.
  • Murakami S; Institute for Chemical Research Kyoto University, 611-0011, Gokasho, Uji, Kyoto, Japan.
  • Sumida Y; Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 101-0062, Kanda- Surugadai, Chiyoda-ku Tokyo, Japan.
  • Hirai G; Graduate School of Pharmaceutical Sciences, Kyushu University, 812-8582, Maidashi, Higashiku, Fukuoka, Japan.
  • Ohmiya H; Institute for Chemical Research Kyoto University, 611-0011, Gokasho, Uji, Kyoto, Japan.
Chemistry ; 30(51): e202402256, 2024 Sep 11.
Article in En | MEDLINE | ID: mdl-38980084
ABSTRACT
We have developed radical C-glycosylation using photoexcitable unprotected glycosyl borate. The direct excitation of glycosyl borate under visible light irradiation enabled the generation of anomeric radical without any photoredox catalysts. The in situ generated anomeric radical was applicable to the radical addition such as Giese-type addition and Minisci-type reaction to introduce alkyl and heteroaryl groups at the anomeric position. In addition, the radical-radical coupling between the glycosyl borate and acyl imidazolide provided unprotected acyl C-glycosides.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Japan