Source:http://linkedlifedata.com/resource/pubmed/id/11250589
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 3
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pubmed:dateCreated |
2001-3-16
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pubmed:abstractText |
The crystalline-state conformation of the title compound, C(29)H(29)NO(9), has been established unequivocally. The R absolute configuration is observed at the 4-methoxyamino moiety and the pyranose ring adopts essentially a perfect (4)C(1) chair. The torsion angle of the exocyclic hydroxymethyl group is shown to be gauche--gauche with respect to O1 and C4, respectively. The conformation along the methoxyamino bond is consistent with that observed for calicheamicin gamma(1)(I).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0108-2701
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
309-10
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading | |
pubmed:year |
2001
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pubmed:articleTitle |
Methyl 2,3,6-tri-O-benzoyl-4-deoxy-4-methoxyamino-alpha-D-glucopyranoside.
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pubmed:affiliation |
LEDSS, UMR CNRS 5616, Université Joseph Fourier, BP 53, 38041 Grenoble CEDEX 9, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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