Source:http://linkedlifedata.com/resource/pubmed/id/19138120
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2009-1-29
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pubmed:abstractText |
The architecturally sophisticated skeleton of the immunosuppressive alkaloid FR901483 was assembled via a process relying on the reaction of an in situ generated imine with a suitably disposed donor-acceptor cyclopropane. A short sequence of functional group transformations provided the natural product in an efficient manner.
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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 |
Feb
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pubmed:issn |
1523-7052
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
5
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
777-9
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pubmed:meshHeading | |
pubmed:year |
2009
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pubmed:articleTitle |
Total synthesis of FR901483.
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pubmed:affiliation |
Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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