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/*
NRC Research Press
Closely based on the ESA journals translator
Copyright (C) 2013 Sebastian Karcher
This program is free software: you can redistribute it and/or modify
it under the terms of the GNU General Public License as published by
the Free Software Foundation, either version 3 of the License, or
(at your option) any later version.
This program is distributed in the hope that it will be useful,
but WITHOUT ANY WARRANTY; without even the implied warranty of
MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
GNU General Public License for more details.
You should have received a copy of the GNU General Public License
along with this program. If not, see <http://www.gnu.org/licenses/>.
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"title": "BORATE COMPLEXING BY FIVE-MEMBERED-RING vic-DIOLS VAPOR PRESSURE EQUILIBRIUM AND N.M.R. SPECTRAL OBSERVATIONS",
"date": "October 1, 1963",
"DOI": "10.1139/v63-354",
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"abstractNote": "Thermometric measurement of vapor pressure equilibria in reaction mixtures containing borate ion and cis-3,4-dihydroxytetrahydrofuran (I) or D-glucose 5,6-carbonate (II) indicate that complexing involves at least three different equilibria. Borate complexing by I is characterized by a gross change in n.m.r. spectral characteristics, most striking being a strong overall decoupling effect. Alterations in the spectrum of II and of 5-O-methyl D-glucose in the presence of borate, when compared with those of D-glucose, suggest that complex formation by the latter sugar proceeds with a pyranose-to-furanose interconversion. The O—C—C—O dihedral angle, within the range 0° to about 40°, does not appear to be a factor determining the stability of borate complexes. Crystalline spirane-type complexes of I, II, and of D-threose have been prepared, illustrating the usefulness of borate complexing for the isolation of some furanose sugars and derivatives.Solutions of alkali tetraborates are found by thermometric vapor pr..., non disponible",
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