| pubmed-article:15049678 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C0441833 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C0524465 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C0205103 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C0028621 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:15049678 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:15049678 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:15049678 | pubmed:dateCreated | 2004-3-30 | lld:pubmed |
| pubmed-article:15049678 | pubmed:abstractText | The preparative and stereoselective synthesis (45-50% overall yields) of the target compound 17 has been accomplished from D-ribose. The bulky protecting groups such as TBDPS and Trityl enforced the facial selectivity during Grignard reaction to give the tertiary beta-allylic alcohol 16 as the sole product, which was oxidatively rearranged to the key molecule 17 in excellent yield. | lld:pubmed |
| pubmed-article:15049678 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15049678 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15049678 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15049678 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15049678 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15049678 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15049678 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15049678 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15049678 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:15049678 | pubmed:issn | 0022-3263 | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:KimHea OkHO | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:JeongLak... | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:MoonHyung... | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:ChoiWon JunWJ | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:ShinDae... | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:LeeJeong AJA | lld:pubmed |
| pubmed-article:15049678 | pubmed:author | pubmed-author:YooByul NaeBN | lld:pubmed |
| pubmed-article:15049678 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15049678 | pubmed:day | 2 | lld:pubmed |
| pubmed-article:15049678 | pubmed:volume | 69 | lld:pubmed |
| pubmed-article:15049678 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15049678 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15049678 | pubmed:pagination | 2634-6 | lld:pubmed |
| pubmed-article:15049678 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:meshHeading | pubmed-meshheading:15049678... | lld:pubmed |
| pubmed-article:15049678 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15049678 | pubmed:articleTitle | Preparative and stereoselective synthesis of the versatile intermediate for carbocyclic nucleosides: effects of the bulky protecting groups to enforce facial selectivity. | lld:pubmed |
| pubmed-article:15049678 | pubmed:affiliation | Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Korea. | lld:pubmed |
| pubmed-article:15049678 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15049678 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
