Source:http://linkedlifedata.com/resource/pubmed/id/17851391
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-9-13
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pubmed:abstractText |
A selective route for the degradation of the unsaturated side chain of ent-labdanes has been devised, giving two useful synthons: 2beta-acetoxy-14,15,17-trinor-ent-labdane-8,13- dione (5) and 2beta-acetoxy-14,15-dinor-ent-labd-8(17)-en-13-one (7), the use of which for the preparation of terpenylquinone derivatives shall be reported elsewhere.
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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:issn |
1420-3049
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
318-27
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pubmed:dateRevised |
2009-10-27
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pubmed:meshHeading | |
pubmed:year |
2007
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pubmed:articleTitle |
Oxidative degradations of the side chain of unsaturated ent-labdanes. Part I.
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pubmed:affiliation |
Departamento de Química, Universidad Técnica Federico Santa María, Av. España No 1680, Valparaíso, Chile. luis.espinozac@usm.cl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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