| pubmed-article:19637860 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19637860 | lifeskim:mentions | umls-concept:C0002062 | lld:lifeskim |
| pubmed-article:19637860 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:19637860 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:19637860 | pubmed:issue | 17 | lld:pubmed |
| pubmed-article:19637860 | pubmed:dateCreated | 2009-8-28 | lld:pubmed |
| pubmed-article:19637860 | pubmed:abstractText | An efficient and flexible synthesis of poison-frog alkaloids 251O and trans-223B has been achieved by using for both alkaloids an enantiodivergent process starting from the common lactam 1. The relative stereochemistry of 251O and trans-223B was determined to be 7 (R = n-C(7)H(15), R' = n-Pr) and 14 by the present enantioselective synthesis. | lld:pubmed |
| pubmed-article:19637860 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19637860 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19637860 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19637860 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19637860 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:19637860 | pubmed:issn | 1520-6904 | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:TezukaYasuhir... | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:KadotaShigeto... | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:DalyJohn WJW | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:ToyookaNaokiN | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:NemotoHideoH | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:SpandeThomas... | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:GarraffoH... | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:ZhouDejunD | lld:pubmed |
| pubmed-article:19637860 | pubmed:author | pubmed-author:Andriamaharav... | lld:pubmed |
| pubmed-article:19637860 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19637860 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:19637860 | pubmed:volume | 74 | lld:pubmed |
| pubmed-article:19637860 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19637860 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19637860 | pubmed:pagination | 6784-91 | lld:pubmed |
| pubmed-article:19637860 | pubmed:dateRevised | 2010-9-13 | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:meshHeading | pubmed-meshheading:19637860... | lld:pubmed |
| pubmed-article:19637860 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19637860 | pubmed:articleTitle | Efficient enantio- and diastereodivergent synthesis of poison-frog alkaloids 251O and trans-223B. | lld:pubmed |
| pubmed-article:19637860 | pubmed:affiliation | Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Sugitani 2630, Toyama 930-0194, Japan. toyooka@pha.u-toyama.ac.jp | lld:pubmed |
| pubmed-article:19637860 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19637860 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19637860 | pubmed:publicationType | Research Support, N.I.H., Intramural | lld:pubmed |
