Linked Life Data

18687007

Source:http://linkedlifedata.com/resource/pubmed/id/18687007

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2008-8-22
pubmed:abstractText
Chemical investigation of the Southern Australian marine brown alga Cystophora moniliformis resulted in the isolation of two new cyclic epimeric terpene diols, moniliforminol A (25) and moniliforminol B (26), a new linear farnesylacetone derivative (27), and the previously described terpenoids 19-24. This study also resulted in the first complete 2D NMR characterization for compounds 21 to 24 as well as the first report of 24 as a natural product. All structures were elucidated by detailed spectroscopic analysis, with the relative configurations of 25 and 26 being established by selective 1D NOE NMR experiments. The absolute configuration of 26 was assigned on the basis of circular dichroism (CD), which also permitted that of 25 to be tentatively assigned.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1520-6025
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1441-6
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
Linear and cyclic C18 terpenoids from the southern Australian marine brown alga Cystophora moniliformis.
pubmed:affiliation
School of Applied Sciences (Discipline of Applied Chemistry), RMIT University, GPO Box 2476V Melbourne, Victoria 3001, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't