Title of article :
A combined X-ray and NMR study of borate esters of furanoidic cis-1,2-diols Original Research Article
Author/Authors :
Klaus Benner، نويسنده , , Peter Klüfers، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2000
Pages :
6
From page :
287
To page :
292
Abstract :
Crystals of K[B(AnErytH−2)2]·2 H2O (AnEryt=1,4-anhydroerythritol) form from aqueous alkaline solutions containing a double molar amount of diol over borate. The spiro-type monoanions are the main borate species in the mother liquors of crystallisation according to 11B and 13C NMR spectroscopy. Ribofuranosides form analogous borate esters using their 1,4-anhydroerythritol core. Crystals of Na[B(Meβ-d-Ribf 2,3H−2)2]·2 H2O were grown from alkaline methyl β-d-ribofuranoside solutions that had attacked boron-containing Duran vessels. NMR spectra show closely resembling borateester speciation in solutions of diols with the 1,4-anhydroerythritol core — 1,4-anhydroerythritol itself, methyl β-d-ribofuranoside and guanosine.
Keywords :
Borate esters , 1 , 4-Anhydroerythritol , Guanosine , Methyl ?-d-ribofuranoside
Journal title :
Carbohydrate Research
Serial Year :
2000
Journal title :
Carbohydrate Research
Record number :
962687
Link To Document :
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