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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1993-9-1
|
| pubmed:abstractText |
Four regioisomeric ditritylated derivatives of cyclomalto-octaose (1, cG8), namely, 6(I),6(n)-di-O-trityl-cG8S have been prepared by the reaction of 1 with chlorotriphenylmethane in pyridine and isolated by high-performance liquid chromatography. The regiochemical determination of the four ditrityl-substituted derivatives has been achieved by means of the "hex-5-enose degradation," followed by examination of the products by fast-atom bombardment-mass spectrometry.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0009-2363
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
41
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
866-9
|
| pubmed:dateRevised |
2000-12-18
|
| pubmed:meshHeading | |
| pubmed:year |
1993
|
| pubmed:articleTitle |
Preparation of di-O-triphenylmethyl-(trityl-)cyclomalto-octaoses, and isolation and characterization by "hex-5-enose degradation" of four positional isomers.
|
| pubmed:affiliation |
Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Japan.
|
| pubmed:publicationType |
Journal Article
|