Literature DB >> 35748909

Synthesis of cyclic α-1,4-oligo-N-acetylglucosamine 'cyclokasaodorin' via a one-pot electrochemical polyglycosylation-isomerization-cyclization process.

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'.

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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


  1 in total

1.  Synthesis of protected precursors of chitin oligosaccharides by electrochemical polyglycosylation of thioglycosides.

Authors:  Md Azadur Rahman; Kana Kuroda; Hirofumi Endo; Norihiko Sasaki; Tomoaki Hamada; Hiraku Sakai; Toshiki Nokami
Journal:  Beilstein J Org Chem       Date:  2022-08-30       Impact factor: 2.544

  1 in total

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