A Short and Simple Synthesis of Branched Mannoligosaccharides with [1-13C]-Labelled Terminal mannose Units

• Autorzy: Ivlev E. , Backinowsky L. , Abronina P. , Kononov L. , Kochetkov N.
• Języki publikacji: EN

Abstrakty

EN

Mannosylation with 2,3,4,6-tetra-O-benzoyl-_-D-[1-13C]mannopyranosyl bromide as a glycosyl donor has been used for the synthesis of 3,6-branched mannotri- and -pentaoside bearing labelled terminal mannopyranose units. Methyl 2,4-di-O-benzoyl-_-Dmannopyranoside was used as the glycosyl acceptor for the synthesis of the trisaccharide and also converted into a disaccharide precursor for the pentasaccharide.

Słowa kluczowe

EN

selective glycosylation; [1-13C]-labelled mannotrioside; [1-13C]-labelled mannopentaosid; synthesis

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Polish Journal of Chemistry
• Rocznik: 2005
• Tom: Vol. 79 / nr 2
• Strony: 275--286
• Opis fizyczny: Bibliogr. 26 poz., rys.

Twórcy

autor

Ivlev E.

• N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation

autor

Backinowsky L.

• N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation

autor

Abronina P.

• N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation

autor

Kononov L.

• N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation

autor

Kochetkov N.

• N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation

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