pubmed-article:11263912 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0185125 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C1176121 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0966287 | lld:lifeskim |
pubmed-article:11263912 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
pubmed-article:11263912 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:11263912 | pubmed:dateCreated | 2001-3-26 | lld:pubmed |
pubmed-article:11263912 | pubmed:abstractText | A novel route to epoxysorbicillinol as well as dimers of sorbicillin is reported. The synthesis is-in principle-amenable to enantioselectivity. The key step is an oxidative dearomatization to produce a stable and highly malleable p-quinol intermediate, which undergoes a highly diastereoselective epoxidation. | lld:pubmed |
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pubmed-article:11263912 | pubmed:language | eng | lld:pubmed |
pubmed-article:11263912 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11263912 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11263912 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11263912 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11263912 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11263912 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11263912 | pubmed:month | Mar | lld:pubmed |
pubmed-article:11263912 | pubmed:issn | 1523-7060 | lld:pubmed |
pubmed-article:11263912 | pubmed:author | pubmed-author:PettusT RTR | lld:pubmed |
pubmed-article:11263912 | pubmed:author | pubmed-author:PettusL HLH | lld:pubmed |
pubmed-article:11263912 | pubmed:author | pubmed-author:Van De... | lld:pubmed |
pubmed-article:11263912 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11263912 | pubmed:day | 22 | lld:pubmed |
pubmed-article:11263912 | pubmed:volume | 3 | lld:pubmed |
pubmed-article:11263912 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11263912 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11263912 | pubmed:pagination | 905-8 | lld:pubmed |
pubmed-article:11263912 | pubmed:dateRevised | 2011-3-23 | lld:pubmed |
pubmed-article:11263912 | pubmed:meshHeading | pubmed-meshheading:11263912... | lld:pubmed |
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pubmed-article:11263912 | pubmed:meshHeading | pubmed-meshheading:11263912... | lld:pubmed |
pubmed-article:11263912 | pubmed:meshHeading | pubmed-meshheading:11263912... | lld:pubmed |
pubmed-article:11263912 | pubmed:meshHeading | pubmed-meshheading:11263912... | lld:pubmed |
pubmed-article:11263912 | pubmed:meshHeading | pubmed-meshheading:11263912... | lld:pubmed |
pubmed-article:11263912 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11263912 | pubmed:articleTitle | Synthesis of (+/-)-epoxysorbicillinol using a novel cyclohexa-2,5-dienone with synthetic applications to other sorbicillin derivatives. | lld:pubmed |
pubmed-article:11263912 | pubmed:affiliation | Department of Chemistry and Biochemistry, University of California at Santa Barbara, Santa Barbara, California 93106, USA. pettus@chem.ucsb.edu | lld:pubmed |
pubmed-article:11263912 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11263912 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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