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rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
6
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|
pubmed:dateCreated |
2009-3-13
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pubmed:abstractText |
A portion of the macrocyclic cembrenoid diterpene providencin possessing conjoined cyclobutane and furancarboxylate units was synthesized from D-glucose using deoxygenative ring contraction methodology to construct the tetrasubstituted cyclobutane and a Knoevenagel condensation of glyceraldehyde to fabricate the trisubstituted furan.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
Mar
|
|
pubmed:issn |
1523-7052
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|
pubmed:author |
|
|
pubmed:issnType |
Electronic
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pubmed:day |
19
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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 |
1433-6
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pubmed:meshHeading |
|
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pubmed:year |
2009
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|
pubmed:articleTitle |
Synthesis of the cyclobutylfuran sector of providencin via zirconium-mediated oxygen abstraction from a furanoside.
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|
pubmed:affiliation |
Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003, USA. james.white@oregonstate.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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