2016
DOI: 10.6060/mhc151198k
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Last Step towards Macrocyclic Glycoterpenoids Having Isosteviol and Glucosamine Moieties

Abstract: The first diglycosides possessing two glucosamine residues and two moieties of diterpenoid isosteviol have beenКлючевые слова: Терпеноиды, изостевиол, глюкозамин, гликоконъюгаты, гликотерпеноиды.

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Cited by 2 publications
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“…The residue was diluted with CH 2 Cl 2 , washed with 5 % NaHCO 3 and water and brine, dried over Na 2 SO 4 ). ‡ Macrocyclic glycoterpenoid (5) ), 5.82 (d, 2H, J = 9.3 Hz, 2NH). NMR experiments were carried out with Avance-400 and Avance-500 (Bruker) spectrometers.…”
Section: Notes and References †mentioning
confidence: 99%
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“…The residue was diluted with CH 2 Cl 2 , washed with 5 % NaHCO 3 and water and brine, dried over Na 2 SO 4 ). ‡ Macrocyclic glycoterpenoid (5) ), 5.82 (d, 2H, J = 9.3 Hz, 2NH). NMR experiments were carried out with Avance-400 and Avance-500 (Bruker) spectrometers.…”
Section: Notes and References †mentioning
confidence: 99%
“…[5] For the macrocyclization of diglycoside 3 its protecting groups were removed by the reaction with activated powdered zinc in glacial acetic acid, and diglycoside 4 were obtained in 87 % yield. † 2 atoms of glucosamine residues were shifted upfield in keeping with the literature data, [6,7] and resonated as a doublet of doublets at 2.…”
mentioning
confidence: 99%