pubmed-article:16247998 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16247998 | lifeskim:mentions | umls-concept:C0205103 | lld:lifeskim |
pubmed-article:16247998 | lifeskim:mentions | umls-concept:C0028621 | lld:lifeskim |
pubmed-article:16247998 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:16247998 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:16247998 | lifeskim:mentions | umls-concept:C1663584 | lld:lifeskim |
pubmed-article:16247998 | pubmed:issue | 5-7 | lld:pubmed |
pubmed-article:16247998 | pubmed:dateCreated | 2005-10-26 | lld:pubmed |
pubmed-article:16247998 | pubmed:abstractText | The preparative and stereoselective synthesis (45- 50% overall yields, >50 g scale) of the key carbasugars 7a-d was achieved from D-ribose via stereoselective Grignard reaction and oxidative rearrangement as key reactions. | lld:pubmed |
pubmed-article:16247998 | pubmed:language | eng | lld:pubmed |
pubmed-article:16247998 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16247998 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16247998 | pubmed:issn | 1525-7770 | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:KimHea OkHO | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:JeongLak... | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:KimHye JinHJ | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:MoonHyung... | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:ChunMoon... | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:ChoiWon JunWJ | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:KimKilhyounK | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:LeeKang ManKM | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:SheenYhun YYY | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:ShinDae... | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:LeeJeong AJA | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:KoYoung MiYM | lld:pubmed |
pubmed-article:16247998 | pubmed:author | pubmed-author:YunMi KyungMK | lld:pubmed |
pubmed-article:16247998 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16247998 | pubmed:volume | 24 | lld:pubmed |
pubmed-article:16247998 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16247998 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16247998 | pubmed:pagination | 611-3 | lld:pubmed |
pubmed-article:16247998 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:16247998 | pubmed:meshHeading | pubmed-meshheading:16247998... | lld:pubmed |
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pubmed-article:16247998 | pubmed:meshHeading | pubmed-meshheading:16247998... | lld:pubmed |
pubmed-article:16247998 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16247998 | pubmed:articleTitle | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides. | lld:pubmed |
pubmed-article:16247998 | pubmed:affiliation | WonJun Choi Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Korea. | lld:pubmed |
pubmed-article:16247998 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16247998 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |