| pubmed-article:18341346 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18341346 | lifeskim:mentions | umls-concept:C0010546 | lld:lifeskim |
| pubmed-article:18341346 | lifeskim:mentions | umls-concept:C0022023 | lld:lifeskim |
| pubmed-article:18341346 | lifeskim:mentions | umls-concept:C0034325 | lld:lifeskim |
| pubmed-article:18341346 | lifeskim:mentions | umls-concept:C0007382 | lld:lifeskim |
| pubmed-article:18341346 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:18341346 | pubmed:dateCreated | 2008-4-10 | lld:pubmed |
| pubmed-article:18341346 | pubmed:abstractText | The regio- and enantioselective cyclization of pyrroles onto N-acyliminium ions generated in situ from hydroxylactams is reported. Modest to excellent ee's and yields are obtained in these novel Pictet-Spengler-type reactions with a chiral thiourea-pyrrole catalyst. Useful synthetic transformations of the versatile pyrroloindolizidinone and pyrroloquinolizidinone products are presented. | lld:pubmed |
| pubmed-article:18341346 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18341346 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18341346 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18341346 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18341346 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18341346 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18341346 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:18341346 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:18341346 | pubmed:author | pubmed-author:JacobsenEric... | lld:pubmed |
| pubmed-article:18341346 | pubmed:author | pubmed-author:RaheemIzzat... | lld:pubmed |
| pubmed-article:18341346 | pubmed:author | pubmed-author:ThiaraParvind... | lld:pubmed |
| pubmed-article:18341346 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18341346 | pubmed:day | 17 | lld:pubmed |
| pubmed-article:18341346 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:18341346 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18341346 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18341346 | pubmed:pagination | 1577-80 | lld:pubmed |
| pubmed-article:18341346 | pubmed:meshHeading | pubmed-meshheading:18341346... | lld:pubmed |
| pubmed-article:18341346 | pubmed:meshHeading | pubmed-meshheading:18341346... | lld:pubmed |
| pubmed-article:18341346 | pubmed:meshHeading | pubmed-meshheading:18341346... | lld:pubmed |
| pubmed-article:18341346 | pubmed:meshHeading | pubmed-meshheading:18341346... | lld:pubmed |
| pubmed-article:18341346 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18341346 | pubmed:articleTitle | Regio- and enantioselective catalytic cyclization of pyrroles onto N-acyliminium ions. | lld:pubmed |
| pubmed-article:18341346 | pubmed:affiliation | Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA. | lld:pubmed |
| pubmed-article:18341346 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18341346 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18341346 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18341346 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18341346 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18341346 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18341346 | lld:pubmed |
