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Volumn 339, Issue 18, 2004, Pages 2895-2899
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An efficient route to thioglycosides with the 2,3-anhydro-D-ribo stereochemistry
a
a
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Author keywords
2,3 Anhydro sugars; Synthesis; Thiofuranosides; Thioglycosides
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Indexed keywords
ANOMERS;
D-XYLOSE;
AROMATIC COMPOUNDS;
STEREOCHEMISTRY;
SYNTHESIS (CHEMICAL);
CARBOHYDRATES;
4 TOLYL 1 THIO ALPHA DEXTRO XYLOFURANOSIDE;
4 TOLYL 1 THIO BETA DEXTRO XYLOFURANOSIDE;
4 TOLYL 2,3 ANHYDRO 1 THIO ALPHA DEXTRO RIBOFURANOSIDE;
4 TOLYL 2,3 ANHYDRO 1 THIO BETA DEXTRO RIBOFURANOSIDE;
4 TOLYL 2,3 ANHYDRO 5 O BENZOYL 1 THIO ALPHA DEXTRO RIBOFURANOSIDE;
4 TOLYL 2,3 ANHYDRO 5 O BENZOYL 1 THIO BETA DEXTRO RIBOFURANOSIDE;
4 TOLYL 2,3,5 TRI O ACETYL 1 THIO ALPHA DEXTRO XYLOFURANOSIDE;
4 TOLYL 2,3,5 TRI O ACETYL 1 THIO BETA DEXTRO XYLOFURANOSIDE;
4 TOLYL 3,5 O SULFINYL 1 THIO ALPHA DEXTRO XYLOFURANOSIDE;
4 TOLYL 3,5 O SULFINYL 1 THIO BETA DEXTRO XYLOFURANOSIDE;
CARBOHYDRATE DERIVATIVE;
THIOGLYCOSIDE;
UNCLASSIFIED DRUG;
XYLOSE;
ARTICLE;
CARBOHYDRATE SYNTHESIS;
METHODOLOGY;
PRIORITY JOURNAL;
STEREOCHEMISTRY;
METHODS;
MOLECULAR CONFORMATION;
THIOGLYCOSIDES;
XYLOSE;
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EID: 9944226661
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/j.carres.2004.10.009 Document Type: Article |
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Times cited : (6)
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References (11)
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