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Volumn 59, Issue 36, 2003, Pages 7203-7214
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Synthesis of anomerically pure vinyl sulfone-modified pent-2-enofuranosides and hex-2-enopyranosides: A group of highly reactive Michael acceptors for accessing carbohydrate based synthons
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Author keywords
Hex 2 enopyranosides; Michael acceptors; Pent 2 enopyranosides; Vinyl sulfone
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Indexed keywords
3 DEOXY 1,2 5,6 DI O ISOPROPYLIDENE 3 C PHENYLSULFONYL ALPHA GLUCOFURANOSE;
FURAN DERIVATIVE;
METHYL 3 DEOXY 3 C 4 TOLYLSULFONYL 5 O TRITYL ALPHA ARABINOFURANOSIDE;
METHYL 3 DEOXY 3 C 4 TOLYLSULFONYL 5 O TRITYL BETA XYLOFURANOSIDE;
METHYL 3 DEOXY 4,6 O (PHENYLMETHYLENE) 3 C PHENYLSULFONYL ALPHA GLUCOPYRANOSIDE;
METHYL 3 DEOXY 4,6 O (PHENYLMETHYLENE) 3 C PHENYLSULFONYL BETA ALLOPYRANOSIDE;
METHYL 3 DEOXY 4,6 O (PHENYLMETHYLENE) 3 C PHENYLSULFONYL BETA GLUCOPYRANOSIDE;
METHYL 5 O BENZYL 3 DEOXY 3 C 4 TOLYLSULFONYL ALPHA ARABINOFURANOSIDE;
METHYL 5 O BENZYL 3 DEOXY 3 C 4 TOLYLSULFONYL ALPHA RIBOFURANOSIDE;
METHYL 5 O BENZYL 3 DEOXY 3 C 4 TOLYLSULFONYL ALPHA XYLOFURANOSIDE;
METHYL 5 O BENZYL 3 DEOXY 3 C 4 TOLYLSULFONYL BETA RIBOFURANOSIDE;
METHYL 5 O BENZYL 3 DEOXY 3 C 4 TOLYLSULFONYL BETA XYLOFURANOSIDE;
PYRANOSIDE;
UNCLASSIFIED DRUG;
XYLOSE;
ARTICLE;
CARBOHYDRATE SYNTHESIS;
DIASTEREOISOMER;
ELIMINATION REACTION;
MICHAEL ADDITION;
OXIDATION;
PRIORITY JOURNAL;
RING OPENING;
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EID: 0041508891
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(03)01059-7 Document Type: Article |
Times cited : (19)
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References (53)
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