| pubmed-article:18044909 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C0027388 | lld:lifeskim |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C0311404 | lld:lifeskim |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C0598128 | lld:lifeskim |
| pubmed-article:18044909 | lifeskim:mentions | umls-concept:C1958069 | lld:lifeskim |
| pubmed-article:18044909 | pubmed:issue | 26 | lld:pubmed |
| pubmed-article:18044909 | pubmed:dateCreated | 2007-12-13 | lld:pubmed |
| pubmed-article:18044909 | 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. | lld:pubmed |
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| pubmed-article:18044909 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18044909 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18044909 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18044909 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18044909 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18044909 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:18044909 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:18044909 | pubmed:author | pubmed-author:PettusThomas... | lld:pubmed |
| pubmed-article:18044909 | pubmed:author | pubmed-author:ReichNorbert... | lld:pubmed |
| pubmed-article:18044909 | pubmed:author | pubmed-author:WuKun-LiangKL | lld:pubmed |
| pubmed-article:18044909 | pubmed:author | pubmed-author:WilkinsonStep... | lld:pubmed |
| pubmed-article:18044909 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18044909 | pubmed:day | 20 | lld:pubmed |
| pubmed-article:18044909 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:18044909 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18044909 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18044909 | pubmed:pagination | 5537-40 | lld:pubmed |
| pubmed-article:18044909 | pubmed:dateRevised | 2011-3-23 | lld:pubmed |
| pubmed-article:18044909 | pubmed:meshHeading | pubmed-meshheading:18044909... | lld:pubmed |
| pubmed-article:18044909 | pubmed:meshHeading | pubmed-meshheading:18044909... | lld:pubmed |
| pubmed-article:18044909 | pubmed:meshHeading | pubmed-meshheading:18044909... | lld:pubmed |
| pubmed-article:18044909 | pubmed:meshHeading | pubmed-meshheading:18044909... | lld:pubmed |
| pubmed-article:18044909 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:18044909 | pubmed:articleTitle | Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition. | lld:pubmed |
| pubmed-article:18044909 | pubmed:affiliation | Department of Chemistry and Biochemistry, University of California at Santa Barbara, Santa Barbara, California 93106-9510, USA. | lld:pubmed |
| pubmed-article:18044909 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18044909 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:18044909 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18044909 | lld:pubmed |
