| Literature DB >> 35748909 |
Hirofumi Endo1, Masaharu Ochi1, Md Azadur Rahman1, Tomoaki Hamada2, Takahiro Kawano2, Toshiki Nokami1,3.
Abstract
Electrochemical synthesis of unnatural cyclic oligosaccharides composed of N-acetylglucosamine with α-1,4-glycosidic linkages has been accomplished. A thioglycoside monomer equipped with the 2,3-oxazolidinone protecting group was used to prepare linear oligosaccharides by electrochemical polyglycosylation. In the same pot, isomerization of the linear oligosaccharides and intramolecular electrochemical glycosylation for cyclization were also conducted sequentially to obtain the precursor of the cyclic α-1,4-oligo-N-acetylglucosamine 'cyclokasaodorin'.Entities:
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Year: 2022 PMID: 35748909 DOI: 10.1039/d2cc02287g
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.065