Linked Life Data

18044909

Source:http://linkedlifedata.com/resource/pubmed/id/18044909

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
26
pubmed:dateCreated
2007-12-13
pubmed:abstractText
A highly selective oxidative [3 + 2] cycloaddition of chiral enol ethers and hydroxynaphthoquinone is described. This convergent strategy is amenable to an enantioselective synthesis of beta-rubromycin and related naphthoquinone spiroketals. Several compounds were found to inhibit DNA-polymerase and telomerase in a manner resembling alpha-rubromycin and beta-rubromycin.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-10487165, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-11506603, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-11742973, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-11854300, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-12657276, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-14602016, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-15760243, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-16706527, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-17020325, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-5447178, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-5764292, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-5955233, http://linkedlifedata.com/resource/pubmed/commentcorrection/18044909-7605428
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1523-7060
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5537-40
pubmed:dateRevised
2011-3-23
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition.
pubmed:affiliation
Department of Chemistry and Biochemistry, University of California at Santa Barbara, Santa Barbara, California 93106-9510, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't