| pubmed-article:15128229 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C0035197 | lld:lifeskim |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C0064582 | lld:lifeskim |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C0439851 | lld:lifeskim |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C1552596 | lld:lifeskim |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C0444454 | lld:lifeskim |
| pubmed-article:15128229 | lifeskim:mentions | umls-concept:C1947931 | lld:lifeskim |
| pubmed-article:15128229 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:15128229 | pubmed:dateCreated | 2004-5-6 | lld:pubmed |
| pubmed-article:15128229 | pubmed:abstractText | An operationally simple oxidative dearomatization of resorcinol derivatives is reported that employs an inexpensive chiral directing group. The method provides access to a variety of p-quinol derivatives in good yield and diastereoselectivity. A short reductive process affords 4-hydroxy-4-alkylcyclohexenone derivatives in excellent yields and enantiomeric excesses. | lld:pubmed |
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| pubmed-article:15128229 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15128229 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15128229 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15128229 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15128229 | pubmed:month | May | lld:pubmed |
| pubmed-article:15128229 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:15128229 | pubmed:author | pubmed-author:PettusThomas... | lld:pubmed |
| pubmed-article:15128229 | pubmed:author | pubmed-author:REISMANJJ | lld:pubmed |
| pubmed-article:15128229 | pubmed:author | pubmed-author:MejoradoLupe... | lld:pubmed |
| pubmed-article:15128229 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15128229 | pubmed:day | 13 | lld:pubmed |
| pubmed-article:15128229 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:15128229 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15128229 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15128229 | pubmed:pagination | 1535-8 | lld:pubmed |
| pubmed-article:15128229 | pubmed:dateRevised | 2011-3-23 | lld:pubmed |
| pubmed-article:15128229 | pubmed:meshHeading | pubmed-meshheading:15128229... | lld:pubmed |
| pubmed-article:15128229 | pubmed:meshHeading | pubmed-meshheading:15128229... | lld:pubmed |
| pubmed-article:15128229 | pubmed:meshHeading | pubmed-meshheading:15128229... | lld:pubmed |
| pubmed-article:15128229 | pubmed:meshHeading | pubmed-meshheading:15128229... | lld:pubmed |
| pubmed-article:15128229 | pubmed:meshHeading | pubmed-meshheading:15128229... | lld:pubmed |
| pubmed-article:15128229 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15128229 | pubmed:articleTitle | Diastereoselective dearomatization of resorcinols directed by a lactic acid tether: unprecedented enantioselective access to p-quinols. | lld:pubmed |
| pubmed-article:15128229 | pubmed:affiliation | Department of Chemistry and Biochemistry, University of California at Santa Barbara, Santa Barbara, California 93106-9150, USA. | lld:pubmed |
| pubmed-article:15128229 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15128229 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15128229 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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