| pubmed-article:17880232 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C0679199 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C1711351 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C1671924 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C1958069 | lld:lifeskim |
| pubmed-article:17880232 | lifeskim:mentions | umls-concept:C0913483 | lld:lifeskim |
| pubmed-article:17880232 | pubmed:issue | 21 | lld:pubmed |
| pubmed-article:17880232 | pubmed:dateCreated | 2007-10-4 | lld:pubmed |
| pubmed-article:17880232 | pubmed:abstractText | An unusual spiroketalization strategy in which a hydroxyalkene serves as a precursor to a cyclic enol ether was applied to the synthesis of the ABCD trioxadispiroketal subunit of azaspiracid-1. The trioxadispiroketal product, which represents a double anomeric effect, was obtained as a single trioxadispiroketal diastereomer. A key ploy in the synthesis of the CD segment was the use of a cyclopropane as a synthon for the C-14 methyl group. | lld:pubmed |
| pubmed-article:17880232 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17880232 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17880232 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17880232 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:17880232 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:17880232 | pubmed:author | pubmed-author:LiXiaohuaX | lld:pubmed |
| pubmed-article:17880232 | pubmed:author | pubmed-author:LiJialiangJ | lld:pubmed |
| pubmed-article:17880232 | pubmed:author | pubmed-author:MootooDavid... | lld:pubmed |
| pubmed-article:17880232 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17880232 | pubmed:day | 11 | lld:pubmed |
| pubmed-article:17880232 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:17880232 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17880232 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17880232 | pubmed:pagination | 4303-6 | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:meshHeading | pubmed-meshheading:17880232... | lld:pubmed |
| pubmed-article:17880232 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17880232 | pubmed:articleTitle | Synthesis of the ABCD trioxadispiroketal subunit of azaspiracid-1: an iodoetherification-dehydroiodination strategy for complex spiroketals. | lld:pubmed |
| pubmed-article:17880232 | pubmed:affiliation | Department of Chemistry, Hunter College, 695 Park Avenue, New York, New York 10065, USA. | lld:pubmed |
| pubmed-article:17880232 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17880232 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
