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pubmed-article:16247998pubmed:dateCreated2005-10-26lld:pubmed
pubmed-article:16247998pubmed:abstractTextThe 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
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pubmed-article:16247998pubmed:authorpubmed-author:KimHea OkHOlld:pubmed
pubmed-article:16247998pubmed:authorpubmed-author:JeongLak...lld:pubmed
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pubmed-article:16247998pubmed:authorpubmed-author:LeeKang ManKMlld:pubmed
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pubmed-article:16247998pubmed:authorpubmed-author:ShinDae...lld:pubmed
pubmed-article:16247998pubmed:authorpubmed-author:LeeJeong AJAlld:pubmed
pubmed-article:16247998pubmed:authorpubmed-author:KoYoung MiYMlld:pubmed
pubmed-article:16247998pubmed:authorpubmed-author:YunMi KyungMKlld:pubmed
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pubmed-article:16247998pubmed:pagination611-3lld:pubmed
pubmed-article:16247998pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16247998pubmed:year2005lld:pubmed
pubmed-article:16247998pubmed:articleTitleStereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides.lld:pubmed
pubmed-article:16247998pubmed:affiliationWonJun Choi Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Korea.lld:pubmed
pubmed-article:16247998pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16247998pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed