1979
DOI: 10.1016/s0008-6215(00)85770-5
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Syn and anti forms of some monosaccharide O-methyl oximes:a 13C-n.m.r. and g.l.c. study

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Cited by 35 publications
(18 citation statements)
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“…Our results are consistent with a previous report by Funcke et al [27]: the E-form is dominating for the aldohexoses (Figure 3a) and for the ketohexoses the ratio between the two forms is almost equal (Figure 3b). In the MS spectra instead (data not shown), the main discriminative feature between the two anomers is the ratio between the ion at m/z 570 and the ion at m/z 480 corresponding to the fragment [M + H-TMSOH] + .…”
Section: Sugarssupporting
confidence: 94%
“…Our results are consistent with a previous report by Funcke et al [27]: the E-form is dominating for the aldohexoses (Figure 3a) and for the ketohexoses the ratio between the two forms is almost equal (Figure 3b). In the MS spectra instead (data not shown), the main discriminative feature between the two anomers is the ratio between the ion at m/z 570 and the ion at m/z 480 corresponding to the fragment [M + H-TMSOH] + .…”
Section: Sugarssupporting
confidence: 94%
“…Peak identifications and mass spectra are given in Table 3. While non‐reducing carbohydrates gave only one chromatographic peak, reducing carbohydrates presented two isomers corresponding to syn and anti or E and Z isomers 28. Gallic acid was also detected and has been described as a natural component of oak wood 19…”
Section: Resultsmentioning
confidence: 99%
“…Funcke and von Sonntag [25] reported that the major O-methyl oximes formed from aldohexoses are the syn forms (which can be an aid in the identification), while for ketohexoses almost equal proportions of syn and anti are formed. Trifluoroacetylated oximes can be prepared at low temperatures and requires low column temperatures for GC but their use is less common [2].…”
Section: Oximesmentioning
confidence: 99%