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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
5-7
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pubmed:dateCreated |
2005-10-26
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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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1525-7770
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pubmed:author |
pubmed-author:ChoiWon JunWJ,
pubmed-author:ChunMoon WooMW,
pubmed-author:JeongLak ShinLS,
pubmed-author:KimHea OkHO,
pubmed-author:KimHye JinHJ,
pubmed-author:KimKilhyounK,
pubmed-author:KoYoung MiYM,
pubmed-author:LeeJeong AJA,
pubmed-author:LeeKang ManKM,
pubmed-author:MoonHyung RyongHR,
pubmed-author:SheenYhun YYY,
pubmed-author:ShinDae HongDH,
pubmed-author:YunMi KyungMK
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pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
611-3
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
|
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pubmed:year |
2005
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pubmed:articleTitle |
Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides.
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|
pubmed:affiliation |
WonJun Choi Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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