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rdf:type |
|
|
lifeskim:mentions |
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pubmed:issue |
10
|
|
pubmed:dateCreated |
2004-5-17
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|
pubmed:abstractText |
The total synthesis of the cytotoxic antitumour natural product epothilone C has provided a stage for the exploitation and further development of immobilized reagent methods. A stereoselective convergent synthetic strategy was applied, incorporating polymer-supported reagents, catalysts, scavengers and catch-and-release techniques to avoid frequent aqueous work-up and chromatographic purification.
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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
|
|
pubmed:month |
May
|
|
pubmed:issn |
0947-6539
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
17
|
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pubmed:volume |
10
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
2529-47
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|
pubmed:dateRevised |
2009-8-4
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|
pubmed:meshHeading |
|
|
pubmed:year |
2004
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|
pubmed:articleTitle |
Multi-step application of immobilized reagents and scavengers: a total synthesis of epothilone C.
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|
pubmed:affiliation |
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
