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Spectra for:
Éva Bozó, Sándor Boros, János Kuszmann
Compound 1 8-BETA
4-O-BENZOYL-5-THIO-BETA-L-ARABINOPYRANOSE;MAJOR_ISOMER
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Compound 11
5-S-BENZOYL_2,3-O-ISOPROPYLIDENE-5-THIO-L-ARABINOSE
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Compound 11-HYDRATE
5-S-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-L-ARABINOSE-HYDRATE
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Compound 12-BETA
4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-BETA-L-ARABINOPYRANOSE
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Compound 14-ALPHA
1-O-ACETYL-4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-ALPHA-L-ARABINOPYRANOSE;MINOR_ISOMER
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Compound 14-BETA
1-O-ACETYL-4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-BETA-L-ARABINOPYRANOSE;MAJOR_ISOMER
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Compound 15-ALPHA
METHYL_2,3-DI-O-ACETYL-4-O-BENZOYL-5-THIO-ALPHA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 15-BETA
METHYL_2,3-DI-O-ACETYL-4-O-BENZOYL-5-THIO-BETA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Compound 20-BETA
2,3-DI-O-ACETYL-4-O-BENZOYL-5-THIO-BETA-L-ARABINOPYRANOSYL_BROMIDE
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Compound 22-ALPHA
4-NITROPHENYL_4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-ALPHA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Compound 22-BETA
4-NITROPHENYL_4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-5-THIO-BETA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 23-ALPHA
4-CYANOPHENYL_4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-1,5-DITHIO-ALPHA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Compound 23-BETA
4-CYANOPHENYL_4-O-BENZOYL-2,3-O-ISOPROPYLIDENE-1,5-DITHIO-BETA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 26-ALPHA
4-CYANOPHENYL_2,3-DI-O-ACETYL-4-O-BENZOYL-1,5-DITHIO-ALPHA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 26-BETA
4-CYANOPHENYL_2,3-DI-O-ACETYL-4-O-BENZOYL-1,5-DITHIO-BETA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Compound 27-ALPHA
4-NITROPHENYL_2,3-DI-O-ACETYL-4-O-BENZOYL-1,5-DITHIO-ALPHA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 27-BETA
4-NITROPHENYL_2,3-DI-O-ACETYL-4-O-BENZOYL-1,5-DITHIO-BETA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Compound 28-ALPHA
4-CYANOPHENYL_1,5-DITHIO-ALPHA-L-ARABINOPYRANOSIDE;MINOR_ISOMER
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Compound 28-BETA
4-CYANOPHENYL-1,5-DITHIO-BETA-L-ARABINOPYRANOSIDE;MAJOR_ISOMER
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Citation
Citation
CARBOHYDR.RES.,311,191(1998)
Journal
Carbohydrate Research
Issue
4
Volume
311
Page(s)
191-202
Year
1998
Author(s)
Éva Bozó, Sándor Boros, János Kuszmann
Publisher
Elsevier BV
DOI
10.1016/S0008-6215(98)00221-3